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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175212Generated: November 3, 2026

Acetyl chloride → Methyl 3-(1-acetylpiperidin-2-yl)-5-(1-cyclohexylethyl)benzoate

https://huagongshe.com/reaction/1175212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68688416HCID 68688416—
CatalystAdams' catalystHCID 345198—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-(1-acetylpiperidin-2-yl)-5-(1-cyclohexylethyl)benzoateHCID 68688722—

Reaction Steps

To an argon purged solution of methyl 3-(1-phenylvinyl)-5-(pyridin-2-yl)benzoate (73 mg, 0.23 mmol) in ethanol (5 mL) and HCl (conc. 1 mL) was added PtO2 (7 mg, 0.023 mmol). The mixture was hydrogenated under a hydrogen atmosphere (35 psi) for 6 h. The reaction mixture was purged with argon, filtered through a 0.2 μm filter, and concentrated. The resulting crude material was taken up with CH2Cl2 (5 mL) after which iPr2NEt (0.1 mL, 0.58 mmol) and acetyl chloride (18 μL, 0.25 mmol) were successively added. The mixture was stirred for 30 min, then diluted with CH2Cl2 (30 mL) and washed successively with 0.5 M HCl (1×10 mL), 9% sodium carbonate (1×10 mL), brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue containing the title compound was used without further purification. MS m/z=372 [M+1]+; Calc'd for C23H33NO3: 371.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838676B2
Source datasetuspto-grants-2010_11
ORD IDord-1e9e9eee4ea24d09a4ceddc83fbd9b55
Source noteuspto-grants-2010_11