Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495052Generated: October 30, 2026

Chlorotrimethylsilane → N-Boc-trans-4-hydroxy-L-prolinol

https://huagongshe.com/reaction/495052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
ProductN-Boc-trans-4-hydroxy-L-prolinolHCID 1127597965%

Reaction Steps

To a 0° C. suspension of LiBH4 (2.0 equiv) in THF (0.67 M) was slowly added TMSCl (4.0 equiv) by syringe. After stirring at room temperature for 30 minutes, (2S,4R)-1-(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid (1.0 equiv) was then added, and the resulting mixture was stirred at room temperature overnight. The reaction was quenched by the careful addition of sat'd. aq. NaHCO3, and the mixture was diluted with EtOAc, and the organice layer was washed twice with sat'd. aq. NaHCO3, once with brine, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The title compound was isolated in 65% yield and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538223B2
Source datasetuspto-grants-2009_05
ORD IDord-50c252175caf44488509e6d1976c63f6
Source noteuspto-grants-2009_05