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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200186Generated: November 1, 2026

Chloroform → 2-(1-Bromocyclohexyl)-8-cyanomethyl-4-oxo-4H-[1]-benzopyran

https://huagongshe.com/reaction/1200186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium CyanideHCID 8929—
Reactant2-(1-Bromocyclohexyl)-8-bromomethyl-4-oxo-4H-[1]-benzopyranHCID 14650439—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventWaterHCID 962—
Product2-(1-Bromocyclohexyl)-8-cyanomethyl-4-oxo-4H-[1]-benzopyranHCID 1465044472.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

NaCN (3.88 g, 0.075 mole) was dissolved in water (11 ml) and to the solution was added benzyltrimethylammonium chloride (13.9 g, 0.075 mole). After stirring at 50° C. for 15 minutes, chloroform (120 ml) was added and further 2 -(1-bromocyclohexyl)-8-bromomethyl-4-oxo-4H-[1]-benzopyran (12 g, 0.03 mole) was added. The mixture was stirred for 4 hours. The chloroform layer was washed with water, dried (MgSO4) and then concentrated under reduced pressure to obtain crystals. The crude crystals were recrystallized from ethyl acetate to obtain the title compound (7.5 g) as prisms, m.p. 143°-144° C., yield 72.2%. IR and NMR spectra of this compound were identical with those of the compound obtained in Reference Example 20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904690
Source datasetuspto-grants-1990_02
ORD IDord-df6218633a364984a6efef2022b93e8d
Source noteuspto-grants-1990_02