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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | Tert-butyl N-[3-oxo-3-(1,3-thiazol-2-YL)propyl]carbamate | HCID 69802122 | — |
| Solvent | 2-Methylpentane | HCID 7892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(3S)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester | HCID 69799613 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953797B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-9ffbe8647db3472f8a14c94b80cf27c2 |
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| Source note | uspto-grants-2005_10 |
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