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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296808Generated: October 31, 2026

Hydrochloric Acid → 4,5-Dihydro-8-methylthio-2-phenylfuro[3,4-e]benzothiazole-6-carboxylic acid

https://huagongshe.com/reaction/2296808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15885622HCID 15885622—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4,5-Dihydro-8-methylthio-2-phenylfuro[3,4-e]benzothiazole-6-carboxylic acidHCID 984102893.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

Ethyl 4,5-dihydro-8-methylthio-2-phenylfuro[3,4-e]benzothiazole-6-carboxylate (1.32 g) was suspended in a mixed solvent of ethanol (10 ml) and tetrahydrofuran (15 ml); a 2 N aqueous solution of sodium hydroxide (5.3 ml) was added at 50° C. After the reaction mixture was stirred at 50° C. for 1.5 hours, the solution obtained was poured over water (300 ml), acidified with concentrated hydrochloric acid, and extracted with ethyl acetate-tetrahydrofuran (3:1, v/v). The organic layer was washed with water and dried (MgSO4), after which the solvent was distilled off to yield 4,5-dihydro-8-methylthio-2-phenylfuro[3,4-e]benzothiazole-6-carboxylic acid (1.14 g, 93.4%), which was then recrystallized from chloroform-methanol. Colorless prisms. Melting point 206-207° C. (decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489351B1
Source datasetuspto-grants-2002_12
ORD IDord-e6cc3e9a3fe943dab476fa811e4681ed
Source noteuspto-grants-2002_12