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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395310Generated: October 30, 2026

4-(2-bromoethoxy)benzenesulfonamide → HCID 18971444, compound

https://huagongshe.com/reaction/2395310

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-bromoethoxy)benzenesulfonamideHCID 4962801—
ReactantHCID 22347443HCID 22347443—
ProductHCID 18971444HCID 18971444—

Reaction Steps

As the starting substances, ethyl 4-chloro-2-phenoxycarbonylaminobenzoate and 4-(2-bromoethyloxy) benzenesulfonamide were used and the same method was applied as in Example 36 to obtain N-[4-(2-bromoethyloxy)benzenesulfonyl]-N'-(2-ethyloxycarbonyl-5-chlorophenyl)urea and further to obtain from 760 mg (1.50 mmol) of N-[4-(2-bromoethyloxy)benzenesulfonyl]-N'-(2-carboxyl-5-chlorophenyl)urea 320 mg of the above-identified compound (yield 46.4%). Properties: colorless crystal, Melting point: >200° C. (decomposition), PMR (δppm, DMSO-d6):3.82 (2H,t), 4.46 (2H,t), 7.12 (1H,s), 7.12-7.23 (3H,m), 7.85 (1H,d), 8.11 (2H,d), 11.59 (1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814631
Source datasetuspto-grants-1998_09
ORD IDord-d07fe62c1d6848b0b1a64b17d4a25f84
Source noteuspto-grants-1998_09