HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971124Generated: October 29, 2026
Water → (S)-tert-Butyl (1-hydroxy-3-methylbutan-2-yl)(methyl)carbamate
https://huagongshe.com/reaction/971124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | Boc-N-methyl-L-valine | HCID 7010608 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-tert-Butyl (1-hydroxy-3-methylbutan-2-yl)(methyl)carbamate | HCID 11790636 | 94% |
Reaction Steps
20.0 g Boc-MeVal-OH (86.5 mmol; Fluka) were dissolved in 80 ml THF and cooled to 0° C. 130 ml 1M BH3-THF (0.13 mol; Fluka) were added at 0° C. over 1 h and the clear, colo reaction mixture was warmed up and stirred at RT for 1 h. The reaction mixture was again cooled to 0° C., 75 ml deionized water were carefully added at 0-5° C. over 0.5 h and after warming up to RT stirring was continued for 1 h. To the colorless solution were added 150 ml 10% Na2CO3 all at once and after stirring for 1 h the reaction mixture was extracted with 600 ml and 300 ml ethyl acetate. The organic layers were washed with brine and dried (Na2SO4). Removal of the solvent by rotary evaporation gave 17.4 g (94%) product as colorless oil. 1H-NMR:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312343B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-859cec6dd58c434a95af38e53a7d858b |
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| Source note | uspto-grants-2007_12 |
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