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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972988Generated: October 30, 2026

2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetamide → 5-oxo-5H-dibenzo[a,d]cyclohepten-2-acetic acid

https://huagongshe.com/reaction/972988

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetamideHCID 20459590—
ReactantChloroform hexaneHCID 21585165—
ReactantAcetone hexaneHCID 21880519—
Product5-oxo-5H-dibenzo[a,d]cyclohepten-2-acetic acidHCID 12398821—

Reaction Steps

3.0 Gm. of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionamide is refluxed in a mixture of 20 ml. of acetic acid and 30 ml. of concentrated hydrochloric acid for 3 hours. The solution is cooled and poured into water. The mixture is extracted with ethyl acetate and the extract is washed, dried and evaporated to yield 90% of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionic acid., m.p. (chloroform-hexane) 138°-139° C.; m.p. (acetone-hexane) 113°-115° C. Use of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetamide gives a similar yield of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetic acid, m.p. (acetone-hexane) 148°-149.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04054579
Source datasetuspto-grants-1977_10
ORD IDord-cd64f74a697147c4974cb8e09caa11ef
Source noteuspto-grants-1977_10