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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477212Generated: October 30, 2026

Trimethylsilyl cyanide → HCID 14181182, compound

https://huagongshe.com/reaction/477212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 14181181HCID 14181181—
CatalystBoron trifluorideHCID 6356—
SolventHydrochloric AcidHCID 313—
ProductHCID 14181182HCID 14181182—

Reaction Steps

2 to 3 drops of BF3 -etherate solution are added to 0.1 mol of methyl 5-oxo-5,6,7,8-tetrahydro-naphth-2-yl-oxyacetate and 0.15 mol of trimethylsilyl cyanide, and the mixture is stirred at room temperature for 30 minutes and then at 50° C. for 1 hour. 250 ml of a saturated methanolic hydrogen chloride solution are added to this solution at room temperature and the mixture is stirred for 1 hour. Some of the product precipitates out and is filtered off. A further batch is obtained by evaporating the motor liquor, taking up the residue in CH2Cl2, extracting the mixture twice by shaking with 0.5N NaOH, drying the extract over Na2SO4 and evaporating it and recrystallizing the residue from a little methanol or diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886898
Source datasetuspto-grants-1989_12
ORD IDord-2e062436b8b14b69bb2b818700d394d0
Source noteuspto-grants-1989_12