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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283656Generated: November 1, 2026

p-Anisoyl chloride → HCID 21510490, compound

https://huagongshe.com/reaction/1283656

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
Reactant2-Butyl-5-chloro-1-benzofuranHCID 13815073—
ProductHCID 21510490HCID 21510490—

Reaction Steps

2-n-Butyl-5-chlorobenzofuran (9.5 g., 0.046 mol.) was acylated with 8 g. (0.047 mol.) of anisoyl chloride as described in the procedure of Example 10 to give 2-n-butyl-5-chloro-3-(4'-methoxybenzoyl)benzofuran. Demethylation followed by reaction of the 2-n-butyl-5-chloro-3-(4'-hydroxybenzoyl)benzofuran with epichlorohydrin and subsequent opening of the epoxy compound formed with isopropylamine was carried out as described in the procedures of Examples 9 and 7 to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975537
Source datasetuspto-grants-1976_08
ORD IDord-69575c389d8f4a13aa32ca521233a617
Source noteuspto-grants-1976_08