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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255519Generated: November 2, 2026

Palmitoyl chloride → HCID 54545161, compound

https://huagongshe.com/reaction/2255519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPalmitoyl chlorideHCID 8206—
ReactantHCID 14668292HCID 14668292—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 54545161HCID 54545161—

Reaction Steps

To a solution of (S)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-3-bromo-2-hydroxy-5,6-dimethoxybenzamide mesylate (0.48 g, 1 mmol) in 10 ml of trifluoroacetic acid was added palmitoyl chloride (0.55 ml, 2 mmol). The reaction mixture was stirred at ambient temperature over molecular sieves for 20 h. After evaporation of the solvent in vacuo ether was added to the residue and filtered. The filtrate was washed several times with a saturated KHCO3 solution and dried (MgSO4). After evaporation of the solvent in vacuo the resulting oil crystallized on cooling. Yield 0.42 g (67%). M.p. 46°-48° C. Rf value is 0.21 for title compound and 0.32 for starting compound (SiO2, TLC-plates, 20% MeOH in i-Pr2O as eluent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240957
Source datasetuspto-grants-1993_08
ORD IDord-2cf5cd173bc548ca8d16607a6fb2a925
Source noteuspto-grants-1993_08