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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852733Generated: October 31, 2026

Triethylamine → HCID 10854740, compound

https://huagongshe.com/reaction/1852733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactanttert-butyl (2S,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-(2-hydroxypropan-2-yl)pyrrolidine-1-carboxylateHCID 86724489—
SolventTolueneHCID 1140—
ProductHCID 10854740HCID 10854740—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of tert-butyl (2S,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-(2-hydroxypropan-2-yl)pyrrolidine-1-carboxylate (98 g) dissolved in toluene (900 mL) at −78° C. was added triethylamine (310 mL). The mixture was stirred at −78° C. for 10 minutes, and then thionyl chloride (60 mL) in toluene (100 mL) was added dropwise over 1.5 hours. The mixture was stirred at −78° C. for 2 hours and then quenched with saturated ammonium chloride. The aqueous layer was extracted with ethyl acetate, and the organic layer was washed with saturated aqueous sodium bicarbonate and brine. The organic layer was dried over sodium sulfate, filtered, and concentrated to give tert-butyl (2S,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-(prop-1-en-2-yl)pyrrolidine-1-carboxylate. The residue was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962611B2
Source datasetuspto-grants-2015_02
ORD IDord-8a393f64c67a43e7889eea820dd53799
Source noteuspto-grants-2015_02