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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604852Generated: October 30, 2026

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

https://huagongshe.com/reaction/604852

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 numberUS07910743B2
Source datasetuspto-grants-2011_03
ORD IDord-3214679b4de743ad98314c5b4527f59d
Source noteuspto-grants-2011_03