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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantBoc-N-methyl-L-valineHCID 7010608—
SolventTetrahydrofuranHCID 8028—
Product(S)-tert-Butyl (1-hydroxy-3-methylbutan-2-yl)(methyl)carbamateHCID 1179063694%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312343B2
Source datasetuspto-grants-2007_12
ORD IDord-859cec6dd58c434a95af38e53a7d858b
Source noteuspto-grants-2007_12