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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329322Generated: October 29, 2026

Water → HCID 20310681, compound

https://huagongshe.com/reaction/329322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbon TetrachlorideHCID 5943—
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
ReactantDiazabicylononeneHCID 66586414—
ProductHCID 20310681HCID 20310681—

Reaction Conditions

Temperature60 °C

Reaction Steps

4.68 G. of 2-carbomethoxy-5-oxo-5H-dibenzo[a,d]-cycloheptane is refluxed in 100 ml. of carbon tetrachloride containing 3.56 g. (1 eq.) of N-bromosuccinimide while being irradiated with a 100 watt incandescent lamp. After 2 hrs. the solution is cooled, filtered and evaporated to dryness. The residue is dissolved in 30 ml. of dimethylformamide and 2.48 g. (1 eq.) of diazabicylononene is added. The mixture is heated briefly to 60° C, and water and ethyl acetate are added. The organic layer is washed with dilute hydrochloric acid and water, then dried and evaporated to give 2-carbomethoxy-5-oxo-5H-dibenzo[a,d]cycloheptene. Hydrolysis in eight to one aqueous methanol, 5% potassium hydroxide, followed by acidification with dilute hydrochloric acid yields 5-oxo-5H-dibenzo[a,d]cycloheptene-2-carboxylic acid (m.p. 261°-262° C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04020094
Source datasetuspto-grants-1977_04
ORD IDord-228eb7108f7b4d408cb62c4f214aa7c3
Source noteuspto-grants-1977_04