Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179951Generated: October 26, 2026

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

https://huagongshe.com/reaction/2179951

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[(3R)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl esterHCID 6980379667.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of (S)-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 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) gave 0.75 g of a clear gum (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887871B2
Source datasetuspto-grants-2005_05
ORD IDord-6abf6e0174e14b47a6980028814fe921
Source noteuspto-grants-2005_05