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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287616Generated: October 29, 2026

Dodecanoyl chloride → HCID 21505557, compound

https://huagongshe.com/reaction/1287616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecanoyl chlorideHCID 8166—
ReactantHCID 114710HCID 114710—
ReactantMaleic AcidHCID 444266—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
SolventChloroformHCID 6212—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 21505557HCID 21505557—

Reaction Steps

In accordance with the general method described in the foregoing Examples, 10.15 grams of 8-ethyl-10-[4-(3-hydroxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin was reacted with a solution of 12.5 grams of lauroyl chloride (dodecanoyl chloride) in a mixture of 60 milliliters of benzene and 20 milliliters of chloroform. By adding a solution of 6.15 grams of maleic acid in 60 milliliters of acetone to the crude product, 14.0 grams of 8-ethyl-10-[4-(3-dodecanoyloxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin di(hydrogen maleate) was recovered. The salt, after recrystallization from acetone, had a melting point of 126°-128°C. Its elemental analysis corresponded to the empirical formula C43H60N2O10S. The free base was obtained in the form of a colorless very viscous oil which was very soluble in vegetable oils by dissolving the salt in a dilute aqueous ammonium hydroxide solution and extracting the resulting solution with benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985750
Source datasetuspto-grants-1976_10
ORD IDord-f0ba1e7c01aa4b7aad538a650eb960ba
Source noteuspto-grants-1976_10