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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972978Generated: October 29, 2026

Acetone Cyanohydrin → 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionitrile

https://huagongshe.com/reaction/972978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone CyanohydrinHCID 6406—
ReactantSodium CyanideHCID 8929—
Reactant2-bromomethyl-5H-dibenzo[a,d]cyclohepten-5-oneHCID 12398819—
SolventDiethyl EtherHCID 3283—
Product2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionitrileHCID 21403095—

Reaction Steps

12.0 Gm. of sodium cyanide and 6.0 gm. of 2-bromomethyl-5H-dibenzo[a,d]cyclohepten-5-one are stirred at 100° C. for 40 minutes in 150 ml. of acetone cyanohydrin. The mixture is cooled and poured into ether. The ethereal layer is washed with water, dried and evaporated. The residue is chromatographed on 350 gm. of silica gel, eluting with hexane/ethyl acetate (3:2) to obtain 8.8 gm., 78%, of 5H-dibenzo[a,d]cyclohepten-5-on-2-yl acetonitrile which is recrystallized from ethyl acetate/hexane, m.p. 119°-121°- C. Use of 2-(α-bromoethyl)-5H-dibenzo[a,d]cyclohepten-5-one gives a similar yield of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionitrile, m.p. 108°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04054579
Source datasetuspto-grants-1977_10
ORD IDord-deae6cbf34f343fbb132b03f98785c4b
Source noteuspto-grants-1977_10