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tert-butyl (1,3-thiazol-4-yl)carbamate

tert-Butyl thiazol-4-ylcarbamate

CAS: 1235406-42-4

Molecular Formula: C8H12N2O2S

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tert-butyl (1,3-thiazol-4-yl)carbamate - Names and Identifiers

Name tert-Butyl thiazol-4-ylcarbamate
Synonyms 100682
4-(BOC-AMINO)-THIAZOLE
tert-butyl thiazol-4-ylcarbamate
tert-Butyl thiazol-4-ylcarbamate
tert-butyl (1,3-thiazol-4-yl)carbamate
tert-Butyl N-(1,3-thiazol-4-yl)carbaMate
tert-butyl thiazol-4-ylcarbamate, Fandachem
(1,3-Thiazol-4-yl)carbamic acid tert-butyl ester
CarbaMic acid, N-4-thiazolyl-, 1,1-diMethylethyl ester
CAS 1235406-42-4

tert-butyl (1,3-thiazol-4-yl)carbamate - Physico-chemical Properties

Molecular FormulaC8H12N2O2S
Molar Mass200.26
Density1.242±0.06 g/cm3(Predicted)
Melting Point153-155 °C
Boling Point254.9±13.0 °C(Predicted)
pKa12.39±0.70(Predicted)
Storage Condition2-8°C
SensitiveIrritant
MDLMFCD18800853

tert-butyl (1,3-thiazol-4-yl)carbamate - Reference Information

Use N-BOC-4-aminothiazole is an organic intermediate, which can be made of thiazol-4-formic acid As a raw material, it is prepared by Curtis rearrangement reaction.
preparation compound thiazole -4-formic acid (15g,116mmol) is dissolved with tert-butanol (750ml), DPPA(47.95g,174mmol) and triethylamine (37.5ml,232mmol) are added, reflux reaction is added at 110 ℃ overnight, and the solvent is dried after the reaction is finished, stir with ethyl acetate (400ml), wash with 5% citric acid solution (200ml), wash with water (200ml), wash with saturated sodium bicarbonate solution (200ml), wash with saturated salt water (200ml), dry with anhydrous sodium sulfate, spin-dry solvent silica gel column chromatography purification (PE/EA = 30:1 → 15:1) to obtain compound N-BOC-4-aminothiazole, white solid 16.2g, yield 69.8%.
Last Update:2024-04-09 21:04:16
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View History
tert-butyl (1,3-thiazol-4-yl)carbamate
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