Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376047Generated: November 4, 2026

Acetyl chloride → HCID 58786545, compound

https://huagongshe.com/reaction/1376047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 58786487HCID 58786487—
SolventDichloromethaneHCID 6344—
SolventSodium BisulfateHCID 516919—
ProductHCID 58786545HCID 5878654516%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 4-[1-(2-Fluoro-phenyl)-2-methylamino-ethyl]-piperazine-1-carboxylic acid tert-butyl ester (425) (0.95 g, 2.81 mmol) in MeCl2(10 mL) was added TEA (0.43 mL, 3.10 mmol). The solution was cooled to 0° C. and allowed to stir for 15 min. Acetyl chloride (0.20 mL, 2.81 mmol) was then added. The reaction was allowed to stir at 0° C. for 35 min and then at room temperature for 132 h. Additional triethylamine (0.39 mL, 2.81 mmol), and acetyl chloride (0.2 mL, 2.81 mmol) were added. The reaction mixture was then diluted with 10% aq. sodium bisulfate (20 mL). The organic layer was separated and the aqueous portion was extracted with dichloromethane (3×). The organics are combined, dried with sodium sulfate and concentrated to dryness. The crude material was purified by chromatography (silica gel 60 mesh, eluting with 2% (2M NH3 in MeOH) in MeCl2) yielding 0.17 g (16%) pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169777B2
Source datasetuspto-grants-2007_01
ORD IDord-3eaae76cd63646e0b3beae3bc7f775ea
Source noteuspto-grants-2007_01