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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384998Generated: November 2, 2026

Water → HCID 523368, compound

https://huagongshe.com/reaction/1384998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactantalpha-Hydroxy-gamma-butyrolactoneHCID 545831—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 523368HCID 52336890%

Reaction Steps

A solution of 10.0 g (98 mmol) of α-hydroxy-γ-butyrolactone in 100 mL of anhydrous THF under argon was cooled to 0-5° C. with magnetic stirring. Addition of 14 mL (110 mmol) of trimethylsilyl chloride and 16 mL (115 mmol) of triethylamine immediately produced a white precipitate. The suspension was warmed to room temperature and stirred for 4 hours. The suspension was poured into a separatory funnel containing 100 mL of H2O and 500 mL of ether. The organic layer was washed with 50 mL of H2O, 50 mL of brine, dried (MgSO4) and concentrated. Purification (Kugelrohr distillation) provided 14.7 g (90% yield) of α-trimethylsilyloxy-γ-butyrolactone bp 80-100° C. (8 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262073B1
Source datasetuspto-grants-2001_07
ORD IDord-fe5a6ba13ab64d2193fd1f3129e68973
Source noteuspto-grants-2001_07