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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075022Generated: November 3, 2026

2-(Dimethylamino)ethanol → beta-Dimethylaminoethyl-10,11-Dihydro-11-oxodibenzo[b,f]thiepin-3-carboxylate

https://huagongshe.com/reaction/1075022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
Reactant3-Chlorocarbonyl-10,11-dihydro-11-oxodibenzo[b,f]thiepinHCID 20270211—
SolventTetrahydrofuranHCID 8028—
Productbeta-Dimethylaminoethyl-10,11-Dihydro-11-oxodibenzo[b,f]thiepin-3-carboxylateHCID 70491159—

Reaction Steps

Dissolve 1.0 gm. of 3-chlorocarbonyl-10,11- dihydro-11-oxodibenzo[b,f]thiepin as prepared in Example 31, Step 1, in 10 cc. of anhydrous tetrahydrofuran with stirring and add 2 ml. of N,N-dimethylethanolamine. Stir at room temperature for 18 hours and strip the mixture to dryness. Partition the residue between ether and dilute hydrochloric acid and separate the aqueous layer. Basify the aqueous layer with aqueous ammonia and extract with ethyl acetate. Evaporate the organic phase and chromatograph the residue over silica-gel eluting with 90% chloroform in methanol to obtain the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04394515
Source datasetuspto-grants-1983_07
ORD IDord-cbaea5d93e44400ab5cd8e118b74929d
Source noteuspto-grants-1983_07