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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256489Generated: October 30, 2026

tert-Butyldimethylsilyl chloride → HCID 12502494, compound

https://huagongshe.com/reaction/256489

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 12653989HCID 12653989—
SolventWaterHCID 962—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 12502494HCID 1250249499.1%

Reaction Steps

Chlorodimethyl-t-butylsilane (485 mg, 3.22 mmol) was added over 5 min to the crude (4S)-enone (7) (247 mg) in hexamethylphosphoric triamide (2 ml) at 0°. After stirring at 4° for 20 h the solution was diluted with water (10 ml) and extracted with ether (3×10 ml). The combined ether extracts were washed with water (3×10 ml), dried (MgSO4) and evaporated to give a pale yellow oil (456 mg) which was chromatographed on a column of silica gel (25 g) with methylene dichloride-methanol (50:1) as eluant. The (4S)-enone (8; R1 =Me2ButSi) [243 mg, 61% from the 3,5,5-trichloro-4-hydroxycyclopent-2-en-1-one (6)] was obtained as a colourless oil, [α]35225 +1050° (c. 9.14×10-2, hexane), [α]23425 -16,140° (c 1.83×10-3, hexane), [θ]33325 +6700° (c 9.14×10-2, hexane), [θ]22225 -80,330° (c 1.83 ×10-3, hexanel). (Found: C, 53.65; H, 7.95; Cl, 14.6. C11H19ClO2Si requires C, 53.55; H, 7.75; Cl, 14.35%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04703127
Source datasetuspto-grants-1987_10
ORD IDord-5dfa369f26954031b5d9a38f082293a2
Source noteuspto-grants-1987_10