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216064-48-1

216064-48-1 Structure

216064-48-1 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL 5-HYDROXY-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE
[CAS]

216064-48-1
[Synonyms]

N-BOC-1,2,3,4-tetrahydro-5-hydeoxy-isoquinoline
TERT-BUTYL 5-HYDROXY-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLAT
tert-butyl 5-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylate
TERT-BUTYL 5-HYDROXY-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE
2-tert-butyloxycarbonyl-5-hydroxy-1,2,3,4-tetrahydroisoquinoline
tert-Butyl 5-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate 95+%
5-Hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-5-hydroxy-, 1,1-dimethylethyl ester
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C14H19NO3
[MDL Number]

MFCD08275037
[MOL File]

216064-48-1.mol
[Molecular Weight]

249.31
Chemical PropertiesBack Directory
[Boiling point ]

378.6±42.0 °C(Predicted)
[density ]

1.170±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

9.96±0.20(Predicted)
[Appearance]

Off-white to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[HazardClass ]

IRRITANT
[HS Code ]

2933491090
Spectrum DetailBack Directory
[Spectrum Detail]

TERT-BUTYL 5-HYDROXY-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE(216064-48-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Di-tert-butyl dicarbonate

24424-99-5

5-Hydroxyisoquinoline

2439-04-5

TERT-BUTYL 5-HYDROXY-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE

216064-48-1

(1) Platinum oxide (100 mg) was added to a solution of 5-hydroxyisoquinoline (2.9 g, 20 mmol) in acetic acid (30 mL) and the hydrogenation reaction was carried out at room temperature and atmospheric pressure. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was crystallized by toluene (20 mL) and collected by filtration. The resulting crystals were dissolved in a solvent mixture of 1 N aqueous sodium hydroxide (40 mL) and tetrahydrofuran (40 mL), followed by addition of di-tert-butyl dicarbonate (4.8 g, 22 mmol). The reaction mixture was stirred at room temperature for 1 h, after which 1 N hydrochloric acid (40 mL) was added. Extraction was carried out with ether, the extract was dried over anhydrous magnesium sulfate and the solvent was removed by evaporation under reduced pressure. The precipitated crystals were recrystallized by diisopropyl ether to give colorless crystals of 2-tert-butoxycarbonyl-5-hydroxy-tetrahydroisoquinoline (2.9 g, 58% yield). Melting point: 163-164 °C. 1H-NMR (CDCl3) δ: 1.49 (9H, s), 2.76 (2H, t, J = 6.0 Hz).

[References]

[1] Patent: EP1123918, 2001, A1
[2] Patent: WO2016/108045, 2016, A2. Location in patent: Page/Page column 29
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