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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085694Generated: October 30, 2026

Dimethylformamide → HCID 86743334, compound

https://huagongshe.com/reaction/1085694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium HydroxideHCID 14798—
ReactantDecanoyl chlorideHCID 66982—
ReactantHCID 20060592HCID 20060592—
ProductHCID 86743334HCID 8674333416%

Reaction Steps

To a stirred and hot (60° C.) solution of 4.2 parts of 4-[(2-benzothiazolyl)methylamino]-α-[(4-fluorophenoxy)methyl]-1-piperidineethanol in 90 parts of N,N-dimethylformamide were added dropwise 2.3 parts of decanoyl chloride. Upon completion, stirring was continued for 24 hours at 60° C. After cooling to room temperature, the reaction mixture was poured onto water and the whole was treated with sodium hydroxide. The aqueous phase was decanted and the residual product was washed three times with water and dissolved in trichloromethane. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the (Z)-2-butenedioate salt in a mixture of 2-propanone and 2,2'-oxybispropane. The salt was filtered off and dried, yielding 1.1 parts (16%) of [2-[4-[(2-benzothiazolyl)methylamino]-1-piperidinyl]-1-[(4-fluorophenoxy)-methyl]ethyl]decanoate (Z)-2-butenedioate(1:1); mp. 134.2° C. (454).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010198
Source datasetuspto-grants-1991_04
ORD IDord-0a578bcd902a4b1cbdb204be382ff909
Source noteuspto-grants-1991_04