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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903633Generated: October 25, 2026

Ethanol → Dibenzo(b,f)thiepin-1-carboxylic acid, 10,11-dihydro-8-methoxy-

https://huagongshe.com/reaction/903633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant9-Carboxy-2-methoxy-10,11-dihydro-11-oxodibenzo[b,f]thiepinHCID 23337037—
Solvent1,4-DioxaneHCID 31275—
ProductDibenzo(b,f)thiepin-1-carboxylic acid, 10,11-dihydro-8-methoxy-HCID 304590329.1%

Reaction Steps

To the mixed solvent of 16 ml of ethanol and 16 ml of dioxane were added 1.8 g of 9-carboxy-2-methoxy-10,11-dihydro-11-oxodibenzo[b,f]thiepin and 2.0 g of hydrazine hydrate and the resulting mixture was heated under reflux for 8 hours. After the completion of reaction, the solvent was distilled off and 1.8 g of sodium hydroxide and 30 ml of diethylene glycol was added to the residue. The thus obtained mixture was heated under reflux at 190°-200° C. for 5 hours. After cooling, water was added to the mixture which was extracted benzene. The aqueous layer was acidified with hydrochloric acid and extracted with benzene. The extract was washed with water, dried and the solvent was distilled off. The thus obtained residue was chromatographed over silica gel, eluted with chloroform-diethylether (10:1), there was obtained 0.5 g of 9-carboxy-2-methoxy-10,11-dihydrodibenzo[b,f]thiepin as colorless needles having a melting point of 185°-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04228284
Source datasetuspto-grants-1980_10
ORD IDord-db54e947aa1e47ada7eeb44a2291f420
Source noteuspto-grants-1980_10