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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834218Generated: October 26, 2026

Water → Phenyl 4-chloro-3-nitrobenzenesulfonate

https://huagongshe.com/reaction/1834218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenolHCID 996—
ReactantBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
ReactantTriethylamineHCID 8471—
SolventAcetoneHCID 180—
ProductPhenyl 4-chloro-3-nitrobenzenesulfonateHCID 26612186.4%

Reaction Steps

3-Nitro-4-Chloro-benzene-sulfonic acid-phenylester was obtained by mixing 51 g of 3-nitro-4-chloro-benzene-sulfonic acid-chloride with 18.8 g of phenol in 120 ml of acetone, and by adding 28 ml of triethylamine dropwise, while cooling, at a temperature not exceeding 10° C. The mixture was continued to be stirred for several hours at room temperature, and then water was added, in which process an oil was separated which was extracted with ether. After recrystallization of the residue from methanol, 54 g of 3-nitro-4-chloro-benzene-sulfonic acid-phenylester were obtained, which had a melting point of 71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04069325
Source datasetuspto-grants-1978_01
ORD IDord-68f9f87caa824dce93a2d5dd5a4266ed
Source noteuspto-grants-1978_01