Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472978Generated: October 30, 2026

N-Methylbenzanilide → Benzyl Alcohol

https://huagongshe.com/reaction/1472978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbenzanilideHCID 74736—
SolventDichloromethaneHCID 6344—
ProductBenzyl AlcoholHCID 24490%
ProductN-MethylanilineHCID 751582%

Reaction Conditions

Temperature100 °C

Reaction Steps

0.01 mmol of the complex 1 produced in Example 1 and 5 mmol of N-methyl-N-phenylbenzamide were placed in a 50 mL-autoclave equipped with a stirrer, and the autoclave was purged with nitrogen. 1.5 mL of Methanol and 2.5 mL of methanol solution of 2.0 M sodium methoxide were added to the autoclave, and the autoclave was purged with hydrogen. The resulting mixture was stirred under hydrogen atmosphere (5 MPa) and 100 degrees C. for 16 hours to obtain a reaction solution. After the completion of reaction, the reaction solution was cooled, diluted with 40 mL of dichloromethane, and subjected to silica gel filtration (eluting solvent: dichloromethane/methanol=10/1). The thus obtained solution was concentrated, and then the resulting residue was purified by silica gel column chromatography (silica gel: 40 g, hexane/ethyl acetate=8/1 to 4/1). As a result, benzyl alcohol (425 mg, 90%) and N-methyl-N-phenylamine (440 mg, 82%) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012690B2
Source datasetuspto-grants-2015_04
ORD IDord-e72a6bf55aea41858d4bca1ac253f816
Source noteuspto-grants-2015_04