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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706800Generated: October 31, 2026

Hydrochloric Acid → 3-[(3-Carboxypropyl)amino]-4-phenoxy-5-sulfamoylbenzoic acid

https://huagongshe.com/reaction/1706800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 70589091HCID 70589091—
SolventWaterHCID 962—
Product3-[(3-Carboxypropyl)amino]-4-phenoxy-5-sulfamoylbenzoic acidHCID 20334534120.7%

Reaction Steps

The chlorobutyramide 3-(γ-chlorobutyrylamino)-4-phenoxy-5-sulfamylbenzoic acid (11.0 g) was added to a solution of KOH (40 g) in water 100 ml. The resulting solution was stirred and heated under reflux overnight. After cooling it was acidified with 3 N acqueous HCl, chilled by adding ice and the product collected, washed and air-dried. A recrystallization from aq. acetone gave 9.80 g (77% on two steps) of N-(2-phenoxy-3-sulfamyl-5-carboxyphenyl)-γ-aminobutyric acid as colorless crystals with m.p. 240°-241°; ir (Nujol) 3400, 3300, 2600 (broad), 1700, 1610, 1590, and 1550 cm-1 ; nmr (CDCl3 /d6 -DMSO) 1.4-2.3 (m, 4H), 3.15 (m, 2H), 4.2 (broad, NH), 6.43 (s, SO2NH2), 6.65-7.4 (m, C6H5), 7.57 (d, J=2, CH), and 7.92 ppm (d, CH); mass spectrum m/e 283 (100%) and 394 (M+ ).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208535
Source datasetuspto-grants-1980_06
ORD IDord-8b695c1ce0794fe283c6154f7a7c32b6
Source noteuspto-grants-1980_06