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4958-02-5

4958-02-5 Structure

4958-02-5 Structure
IdentificationBack Directory
[Name]

3-benzyloxy-cyclobutanecarboxylic acid
[CAS]

4958-02-5
[Synonyms]

3-benzyloxy-cyclobutanecarboxylic
3-benzyloxy-cyclobutanecarboxylic acid
3-Benzyloxycyclobutanecarboxylicacid,97%
3-(benzyloxy)cyclobutane-1-carboxylic acid
3-(phenylmethoxy)-1-cyclobutanecarboxylic acid
3-(phenylmethoxy)cyclobutane-1-carboxylic acid
Cyclobutanecarboxylic acid, 3-(phenylmethoxy)-Cyclobutanecarboxylic acid, 3-(benzyloxy)-(6CI,7CI,8CI)
[Molecular Formula]

C12H14O3
[MDL Number]

MFCD00512751
[MOL File]

4958-02-5.mol
[Molecular Weight]

206.238
Chemical PropertiesBack Directory
[Boiling point ]

194 °C(Press: 6 Torr)
[density ]

1.19
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

4.48±0.40(Predicted)
[Appearance]

White to off-white Solid
[InChI]

1S/C12H14O3/c13-12(14)10-6-11(7-10)15-8-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2,(H,13,14)
[InChIKey]

YNNOFVDQHAHVFG-UHFFFAOYSA-N
[SMILES]

O=C(O)C(C1)CC1OCC2=CC=CC=C2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

2916200090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Hazard InformationBack Directory
[Uses]

3-Benzyloxycyclobutanecarboxylic acid is a useful building block for organic synthesis.
[Synthesis]

3-(BENZYLOXY)CYCLOBUTANE-1,1-DICARBOXYLIC ACID

84182-46-7

3-benzyloxy-cyclobutanecarboxylic acid

4958-02-5

General procedure for the synthesis of 3-benzyloxy-cyclobutanecarboxylic acid from 3-benzyloxycyclobutane-1,1-dicarboxylic acid: 3-(benzyloxy)cyclobutane-1,1-dicarboxylic acid (1.5 g, 5.99 mmol) was dissolved in pyridine (3 mL) and the reaction was heated for 12 h at 120 °C in an oil bath. Upon completion of the reaction, the reaction mixture was cooled to room temperature and the pyridine was evaporated under reduced pressure. Subsequently, toluene (10 mL) was added to the residue and the resulting solution was washed with 1N hydrochloric acid solution (3 times), the organic phase was dried over anhydrous magnesium sulfate, filtered, and then concentrated under reduced pressure to give the brown oily target product 3-benzyloxy-cyclobutanecarboxylic acid (1.17 g, 95% yield).

[References]

[1] Patent: WO2011/143366, 2011, A1. Location in patent: Page/Page column 44
[2] Helvetica Chimica Acta, 1992, vol. 75, # 2, p. 589 - 603
[3] Collection of Czechoslovak Chemical Communications, 1982, vol. 47, # 9, p. 2440 - 2447
[4] Patent: WO2007/62332, 2007, A2. Location in patent: Page/Page column 17
[5] Patent: WO2007/62333, 2007, A2. Location in patent: Page/Page column 12
Spectrum DetailBack Directory
[Spectrum Detail]

3-benzyloxy-cyclobutanecarboxylic acid(4958-02-5)1HNMR
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