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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185913Generated: October 25, 2026

Water → N-[2-(4-Chlorophenyl)-4-hydroxybutyl]-N-methyl-5,6,7,8-tetrahydro-1-naphthamide

https://huagongshe.com/reaction/2185913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5,6,7,8-Tetrahydronaphthalene-1-carbonyl chlorideHCID 2753162—
Reactant3-(4-chloropenyl)-N-methyl-4-amino-1-butanolHCID 22622327—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
ProductN-[2-(4-Chlorophenyl)-4-hydroxybutyl]-N-methyl-5,6,7,8-tetrahydro-1-naphthamideHCID 2245264890.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred cooled (0° C.) mixture of 3-(4-chloropenyl)-N-methyl-4-amino-1-butanol (0.706 g, 3.30 mmol) in DCM (25 mL) and 1N NaOH (4.13 mL) was added dropwise a solution of 5,6,7,8-tetrahydro-1-naphthalenecarbonyl chloride (0.643 g, 3.30 mmol) in DCM (10 mL). The mixture was stirred at 0° C. for 2.5 h, H2O and DCM were added and the mixture was extracted with DCM (2×20 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated in vacuo. Purification by chromatography (0%, 50%, 100% EtOAc in Et2O) provided the title compound (1.11 g, 90%) as a solid. MS m/z 372 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403601B1
Source datasetuspto-grants-2002_06
ORD IDord-b41b220a3234487b93a072a95b1fe95f
Source noteuspto-grants-2002_06