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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459676Generated: November 2, 2026

p-Anisoyl chloride → HCID 53929772, compound

https://huagongshe.com/reaction/1459676

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantHCID 54224308HCID 54224308—
SolventDichloromethaneHCID 6344—
ProductHCID 53929772HCID 5392977295%

Reaction Steps

Triethylamine (28 mg, 0.28 mmol) and anisoyl chloride (47 mg, 0.28 mmol) were added to a solution of 5-amino-2-n-butyl-3-(3,5-diiodo-4-ethyl carboxymethoxybenzoyl)-benzofuran (prepared as in Example 1(g) (150 mg, 0.23 mmol) in methylene chloride (5 ml) . The resulting mixture was stirred at room temperature overnight, then washed with brine, dried using MgSO4 and concentrated to produce 172 mg (95%) of 2-n-butyl-3-(3,5-diiodo-4-ethyl carboxymethoxybenzoyl)-5-(4-methoxybenzamido)benzofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854282
Source datasetuspto-grants-1998_12
ORD IDord-6bf3e3572c084361ba932410cf5b02f1
Source noteuspto-grants-1998_12