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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646602Generated: November 3, 2026

Chlorotrimethylsilane → HCID 19801182, compound

https://huagongshe.com/reaction/1646602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylamineHCID 7912—
ReactantHCID 19801174HCID 19801174—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19801182HCID 19801182—

Reaction Steps

1.24 ml of diisopropylamine and 6 ml of tetrahydrofuran are cooled to -40° C., then 4.7 ml of butyllithium is added drop by drop. The temperature is allowed to rise to -20° C., agitation is carried out for 1/4 hour, then 1 g of 4-(2-propenyl)-1-indanone in 10 ml of tetrahydrofuran is introduced at -70° C. After agitation for one hour at -60° C., 1.15 ml of trimethylsilyl chloride in 6 ml of tetrahydrofuran is added, with agitation for one hour at -60° C. The mixture is poured over 100 ml of water and ice and 100 ml of ether. After decanting, the aqueous phase is extracted with ether, the organic phases are reunited, dried and concentrated to dryness without heating, and 1.51 g of expected product is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180741
Source datasetuspto-grants-1993_01
ORD IDord-f3bb77fb21a14bc19754733118689c8c
Source noteuspto-grants-1993_01