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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077021Generated: October 27, 2026

Hydrogen Sulfide → HCID 178526134, compound

https://huagongshe.com/reaction/1077021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
ReactantPhenolphthaleinHCID 4764—
ReactantSodium HydroxideHCID 14798—
Reactant2-Iodobenzoyl chlorideHCID 69112—
SolventWaterHCID 962—
ProductHCID 178526134HCID 178526134—

Reaction Steps

A solution of sodium hydroxide (10.68 g) in water (14 ml) and alcohol (55 ml) was stirred and treated with hydrogen sulphide at 20° until the mixture did not give an immediate alkaline reaction with phenolphthalein. The solution was cooled to 10°-15° and treated slowly with o-iodobenzoyl chloride (33.66 g). The mixture was stirred for 11/4 hours. The precipitated sodium chloride was filtered off and washed with ethanol (25 ml.) The filtrate was concentrated slightly in vacuo and treated with cold water (80 ml). The solution was covered with ether (100 ml) and stirred while the pH was adjusted to 1.3 with 2N-hydrochloric acid. The ether layer was separated and the aqueous layer was further extracted with ether. The combined ether extracts were washed with water and dried. The ether solution was mixed with water and adjusted to pH 7 with dilute sodium hydroxide solution. The aqueous layer was separated, swirled briefly in vacuo and freeze dried. Trituration of the freeze dried product with ether gave the title compound (28.6 g) as a pale yellow solid. νmax. (Nujol) 15.32 cm-1 (COS-).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959260
Source datasetuspto-grants-1976_05
ORD IDord-226722e26e8941a2a4f10ebad0c9aca7
Source noteuspto-grants-1976_05