Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276214Generated: November 1, 2026

Sodium Hydroxide → HCID 67483509, compound

https://huagongshe.com/reaction/276214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67482961HCID 67482961—
SolventEthanolHCID 702—
ProductHCID 67483509HCID 6748350999.5%

Reaction Conditions

Temperature47.5 °C

Reaction Steps

A solution of (E)-3-cyclohexyl-2-(3-chloro-4-((methylene)-methylsulfonyl)-phenyl)-acrylic acid methyl ester (887 mg, 2.4 mmol) in ethanol (10 mL) was treated with a 1N aqueous sodium hydroxide solution (8 mL). The solution was heated at 45-50° C. for 15 h, at which time, thin layer chromatography analysis of the reaction mixture indicated the absence of starting material. The reaction mixture was concentrated in vacuo to remove ethanol. The residue was diluted with water (20 mL) and extracted with diethyl ether (1×50 mL) to remove any neutral impurities. The aqueous layer was then acidified with a 1N aqueous hydrochloric acid solution, and the resulting acid was extracted into ethyl acetate (2×50 mL). The combined organic layers were washed with a saturated aqueous sodium chloride solution (1×100 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford the (E)-3-cyclohexyl-2-(3-chloro-4-((methylene)-methylsulfonyl)-phenyl)-acrylic acid (0.847 g, 99%) as a white solid: mp 105-108° C.; EI-HRMS m/e calcd for C17H21ClO4S (M+) 356.0849, found 356.0844.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353111B1
Source datasetuspto-grants-2002_03
ORD IDord-397c5681047c44da9ba4dd33c8a364d3
Source noteuspto-grants-2002_03