Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585215Generated: November 1, 2026

Benzoyl chloride → HCID 14435469, compound

https://huagongshe.com/reaction/1585215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant3-PhenylindoleHCID 96502—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14435469HCID 1443546992.8%

Reaction Conditions

Temperature-25 °C

Reaction Steps

In 400 ml of tetrahydrofuran, 42.0 g of 3-phenyl indole was solved. The solution and 25.0 g of potassium tert-butoxide added thereto at -30--20° C. were together heated to normal room temperature and stirred for 30 minutes. The reaction solution was cooled to -20--10° C. and 26 ml of benzoyl chloride added thereto were together heated to normal room temperature and stirred for one hour. The resultant mixture was poured into ice water and extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate, distilled to expel the chloroform, crystallized by addition of isopropyl ether, separated by filtration, and dried to obtain 60.0 g of 1-benzoyl-3-phenylindole (92.8%) having a melting point of 154-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05936098
Source datasetuspto-grants-1999_08
ORD IDord-82121b6e81094b6e895e9bf985be0c44
Source noteuspto-grants-1999_08