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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046419Generated: October 30, 2026

Imidazole → [3-(tert-Butyl-silanoxy)-1-(S)-methyl-propyl]-carbamic acid benzyl ester

https://huagongshe.com/reaction/1046419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactantbenzyl N-[(2S)-4-hydroxybutan-2-yl]carbamateHCID 66849810—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product[3-(tert-Butyl-silanoxy)-1-(S)-methyl-propyl]-carbamic acid benzyl esterHCID 131730925114.6%

Reaction Steps

(3-Hydroxy-1-(S)-methyl-propyl)-carbamic acid benzyl ester (8.02 g, 35.9 mmol) was taken up in DMF (75 mL). tert-Butyl-dimethylsilyl chloride (8.12 g, 53.9 mmol) was added to the solution followed by imidazole (4.15 g, 61.0 mmol). The reaction was stirred at rt and monitored by TLC. The reaction was determined to be complete at 1 h by TLC. The reaction was taken up in EtOAc (200 mL) and partitioned between 5% LiCl(aq) (200 mL). The aqueous was back extracted with EtOAc. The organics were combined and washed with 3×200 mL 5% LiCl(aq), and dried over Na2SO4. Solids were filtered and solvent removed under reduced pressure. [3-(tert-Butyl-silanoxy)-1-(S)-methyl-propyl]-carbamic acid benzyl ester (12.73 g, 100%) was isolated by silica gel chromatography as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569302B2
Source datasetuspto-grants-2013_10
ORD IDord-9dc55537fc694e00ac69cfb289acf66f
Source noteuspto-grants-2013_10