Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966962Generated: October 26, 2026

Methanol → [(3S)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester

https://huagongshe.com/reaction/966962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetateHCID 8857—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantTert-butyl N-[3-oxo-3-(1,3-thiazol-2-YL)propyl]carbamateHCID 69802122—
Solvent2-MethylpentaneHCID 7892—
SolventTetrahydrofuranHCID 8028—
Product[(3S)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl esterHCID 6979961367%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of (R)-3-methyl-CBS-oxazaborolidine (1M solution in toluene, 0.43 ml) in dry tetrahydrofuran (30 ml) at −10° C. under nitrogen, was added borane-tetrahydrofuran complex (1M in tetrahydrofuran, 2.58 ml) and the mixture was stirred at −10° C. for 15 minutes. A solution of [3-oxo-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester (1.1 g, 4.3 mmol) in dry tetrahydrofuran (20 ml) was added dropwise over 45 minutes and the resulting mixture was allowed to warm up to room temperature over 16 h. Methanol (10 ml) was added and the mixture was stirred at room temperature for 15 minutes before the solvent was removed at reduced pressure. Methanol (10 ml) was again added and removed at reduced pressure to leave a crude yellow oil. Flash chromatography (silica, 25 to 100% ethyl acetate in isohexane) afforded a clear gum (0.74 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953797B2
Source datasetuspto-grants-2005_10
ORD IDord-9ffbe8647db3472f8a14c94b80cf27c2
Source noteuspto-grants-2005_10