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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986042Generated: November 2, 2026

p-Anisoyl chloride → HCID 178488838, compound

https://huagongshe.com/reaction/986042

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantHCID 21272654HCID 21272654—
SolventDichloromethaneHCID 6344—
ProductHCID 178488838HCID 178488838—

Reaction Steps

2.8 g (13.6 mmol) 5,6-diamino-3-isopropylindolin-2-one dihydrochloride were suspened in 10 ml. methylene chloride, mixed with 2.55 g. (15 mmol) p-methoxybenzoyl chloride and 4.55 g. (45 mmol) triethylamine added dropwise thereto at 25° C. The reaction mixture was stirred for 2 hours, evaporated and worked up with water. The residue was heated under reflux for about 24 hours in 75 ml. ethanol and 75 ml. concentrated hydrochloric acid, evaporated and rendered neutral with 2N ammonia solution. The residue filtered off with suction was recrystallised from ethyl acetate/methanol. There were obtained 2.1 g. (48.2% of theory) of the title compound; m.p. 326°-328° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04710510
Source datasetuspto-grants-1987_12
ORD IDord-8fa163ff1fa644a3869a19bec95a5f33
Source noteuspto-grants-1987_12