ChemicalBook--->CAS DataBase List--->85272-31-7

85272-31-7

85272-31-7 Structure

85272-31-7 Structure
IdentificationMore
[Name]

DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)
[CAS]

85272-31-7
[Synonyms]

DI-T-BUTYLSILYLBIS(TRIFLUOROMETHANESULFONATE)
DI(T-BUTYL)SILYL BIS(TRIFLUOROMETHANESULPHONATE)
DI-T-BUTYLSILYL DITRIFLATE
DI-TERT-BUTYLBIS(TRIFLUOROMETHANESULFONYLOXY)SILANE
DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)
DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULPHONATE)
DI-TERT-BUTYLSILYL DITRIFLATE
DTBS DITRIFLATE
TRIFLUOROMETHANESULFONIC ACID DI-TERT-BUTYLSILYLENE ESTER
Di-t-butylsilybis(trifluoromethanesulfonate
Methanesulfonic acid, trifluoro-, bis(1,1-dimethylethyl)silylene ester
BIS(TRIFLUOROMETHANESULFONATE)
Di-tert-butylsilyl ditriflate, DTBS ditriflate, Trifluoromethanesulfonic acid di-tert-butylsilylene ester
Bis(trifluoromethanesulfonic acid)[di(1,1-dimethylethyl)silanediyl] ester
Bis(trifluoromethanesulfonic acid)di-tert-butylsilanediyl ester
Di-tert-butylbis(trifluoromethylsulfonyloxy)silane
[EINECS(EC#)]

680-172-7
[Molecular Formula]

C10H18F6O6S2Si
[MDL Number]

MFCD00010581
[Molecular Weight]

440.45
[MOL File]

85272-31-7.mol
Chemical PropertiesBack Directory
[Boiling point ]

73-75 °C/0.35 mmHg (lit.)
[density ]

1.352 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.398(lit.)
[Fp ]

195 °F
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

sol most common organic solvents.
[form ]

Oil
[color ]

Clear Pale Yellow
[Specific Gravity]

1.358
[Hydrolytic Sensitivity]

8: reacts rapidly with moisture, water, protic solvents
[BRN ]

3569211
[Stability:]

Moisture Sensitive
[InChI]

InChI=1S/C10H18F6O6S2Si/c1-7(2,3)25(8(4,5)6,21-23(17,18)9(11,12)13)22-24(19,20)10(14,15)16/h1-6H3
[InChIKey]

HUHKPYLEVGCJTG-UHFFFAOYSA-N
[SMILES]

C(F)(F)(F)S(O[Si](C(C)(C)C)(C(C)(C)C)OS(C(F)(F)F)(=O)=O)(=O)=O
[CAS DataBase Reference]

85272-31-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P280-P301+P330+P331-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
[Hazard Codes ]

C
[Risk Statements ]

R34:Causes burns.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 3265 8/PG 2
[WGK Germany ]

3
[F ]

10-21
[Hazard Note ]

Corrosive
[TSCA ]

No
[REACH Registrations]

Active
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29319090
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Skin Corr. 1B
Hazard InformationBack Directory
[Chemical Properties]

Colorless to yellow liquid
[Physical properties]

bp 73–75°C/0.35 mmHg; d 1.208 g cm?3.
[Uses]

Di-t-butylsilyl bis(trifluoromethanesulfonate) is a reagent for the selective protection of polyhydroxy compounds. This reagent reacts with 1,2-, 1,3-, and 1,4-diols under mild conditions to give the corresponding dialkylsilylene derivatives in high yield (0–50°C, 79–96%). Deprotection is conveniently achieved by using aqueous hydrofluoric acid in acetonitrile (eq 1).
Unlike di-t-butyldichlorosilane, this reagent reacts with hindered alcohols. Even pinacol reacts to give the silylene derivative (100°C, 24 h, 70%). Di-t-butylsilylene derivatives of 1,2-diols are more reactive than those of 1,3- and 1,4-diols and undergo rapid hydrolysis (5 min) in THF/H2O at pH 10, while the 1,3- and 1,4- derivatives are unaffected at pH 4–10 (22°C) for several hours. This protecting group is stable under the conditions of PDC oxidation of alcohols (CH2Cl2, 25?C, 27 h) and tosylation of alcohols (pyridine, 25°C, 27 h).
The reagent has seen limited use for the protection of alcohols but has been used to protect nucleosides (eq 2).The procedure consists of sequential addition of the ditriflate and triethylamine to the nucleoside in DMF. The choice of solvent is critical.

[Preparation]

by the treatment of di-t-butylchlorosilane with trifluoromethanesulfonic acid, followed by distillation (71% yield).
Spectrum DetailBack Directory
[Spectrum Detail]

DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)(85272-31-7)1HNMR
DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)(85272-31-7)Raman
DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)(85272-31-7)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

85272-31-7(sigmaaldrich)
[TCI AMERICA]

Di-tert-butylsilyl Bis(trifluoromethanesulfonate),>97.0%(T)(85272-31-7)
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