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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287613Generated: October 27, 2026

Octanoyl chloride → HCID 21505558, compound

https://huagongshe.com/reaction/1287613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctanoyl chlorideHCID 8124—
Reactant3-{4-[8-(Methylsulfanyl)-10,11-dihydrodibenzo[b,f]thiepin-10-yl]piperazin-1-yl}propan-1-olHCID 147577—
SolventBenzeneHCID 241—
SolventChloroformHCID 6212—
ProductHCID 21505558HCID 21505558—

Reaction Conditions

Temperature60 °C

Reaction Steps

In accordance with the general procedure described in the foregoing Examples, 14.0 grams of 8-methylthio-10-[4-(3-hydroxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin was reacted with 12.2 grams of caprylyl chloride (octanoyl chloride) in a mixture of 20 milliliters of chloroform and 60 milliliters of benzene. After the reaction mixture had been allowed to stand for 4 days at room temperature, the reaction mixture was heated to a temperature of 60°C and further treated as described in the preceding Example. The recovered crude 8-methylthio-10-[4-(3-octanoyloxypropyl)piperazino]-10,11-dihydrodibenzo[b,f]thiepin was thereafter converted into the crystalline di(hydrogen maleate) as described in the foregoing Example. The salt was recovered in a yield of 13.7 grams and, after recrystallization from acetone, had a melting point of 122°-123°C. The pure base was recovered in the form of a viscous oil by treatment of the pure salt with a dilute aqueous solution of ammonium hydroxide as described in the foregoing Example.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985750
Source datasetuspto-grants-1976_10
ORD IDord-522442931e4a4ce393a570d552b1071a
Source noteuspto-grants-1976_10