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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649943Generated: November 1, 2026

Hydrochloric Acid → HCID 19855485, compound

https://huagongshe.com/reaction/1649943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14014982HCID 14014982—
ProductHCID 19855485HCID 19855485—

Reaction Steps

10 mmol of 6-amino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetic acid and 20 mmol of benzenesulphonyl chloride are warmed at 80° C. in 40 ml of 10% strength NaOH for 2 hours. The mixture is then acidified with concentrated HCl and the milky suspension is extracted by shaking twice with ethyl acetate. The combined ethyl acetate phases are rapidly extracted by shaking with 10% strength NaOH (product precipitates out of the ethyl acetate), the NaOH phase is acidified with concentrated HCl and extracted by shaking twice with ethyl acetate and the extract is dried over Na2SO4 and evaporated. The residue is boiled up in ethyl acetate and the mixture is filtered. The product crystallizes out after 2-3 hours in a refrigerator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921998
Source datasetuspto-grants-1990_05
ORD IDord-e58b00c2a52344b7bb3d9f15087a319d
Source noteuspto-grants-1990_05