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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383295Generated: November 1, 2026

Benzoyl chloride → HCID 9800735, compound

https://huagongshe.com/reaction/1383295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 9947928HCID 9947928—
SolventDichloromethaneHCID 6344—
ProductHCID 9800735HCID 980073579%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzoyl chloride (0.49 g, 3.5 mmol) was added to a solution of 1-(2-methoxyphenyl)-4-piperidin-3-ylmethyl-piperazine (1.0 g, 3.5 mmol) from example 6 and triethylamine (2 equivalents, 1 mL) in CH2Cl2 (30 mL) and the solution stirred under N2 at 0° C. for 16 hours. The mixture was concentrated under vacuum, water (50(mL) added and the product extracted into ethyl acetate (3×25 mL). The combined organics were washed with water (25 mL), saturated sodium bicarbonate (20 mL) and brine (25 mL). After drying over sodium sulfate, filtration and concentration under vacuum afforded the titled product (1.08 g, 79% yield). An ethanolic solution of the product was treated

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255302B1
Source datasetuspto-grants-2001_07
ORD IDord-3cd4c08fb8e74423b4f14de952ca8d5d
Source noteuspto-grants-2001_07