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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398535Generated: October 30, 2026

p-Anisoyl chloride → HCID 21433227, compound

https://huagongshe.com/reaction/2398535

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 21433224HCID 21433224—
ProductHCID 21433227HCID 21433227—

Reaction Steps

2-Amino-4-trifluoromethyl-5-bromo-benzenesulfonamide (formula (V): R2 = Br) is first prepared according to the above-described technique. M.p.= 202° C. The 2-amino-4-trifluoromethyl-5-bromobenzenesulfonamide (9.60 g) is then reacted, as in Example 2A, with p-anisic acid chloride (6.8 g), to give 12.2 g 2-p-anisoylamino-4-trifluoromethyl-5-bromo-benzenesulfonamide, M.p.= 321° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025508
Source datasetuspto-grants-1977_05
ORD IDord-9cb1bd12b84343c8a2309c37984764f9
Source noteuspto-grants-1977_05