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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194818Generated: November 4, 2026

Benzoyl Peroxide → HCID 21268557, compound

https://huagongshe.com/reaction/1194818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 21268558HCID 21268558—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 21268557HCID 21268557—

Reaction Steps

7-(4-Methylthiobenzoyl)-2,3-dihydrobenzofuran-5-ylacetic acid (1.0 g) was heated at reflux in carbon tetrachloride (100 ml) containing n-bromosuccinimide (0.54 g) and a catalytic quantity of benzoyl peroxide. After approximately 2 hours the reaction mixture was cooled and extracted with dilute aqueous sodium carbonate. The aqueous extract was acidified with hydrochloric acid, extracted with ethyl acetate, dried and evaporated to yield a residue which was crystallized from acetone/hexane to give (7-(4-methylthiobenzoyl)benzofuran-5-ylacetic acid, m.p. --151°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816473
Source datasetuspto-grants-1989_03
ORD IDord-022070fdebc44b229dac808c37b43775
Source noteuspto-grants-1989_03