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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828960Generated: November 2, 2026

Hydrochloric Acid → Benzeneethanamine, 3,4-dimethoxy-N,alpha-dimethyl-

https://huagongshe.com/reaction/1828960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
Reactant2-Propanone, 1-(3,4-dimethoxyphenyl)-HCID 69896—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductBenzeneethanamine, 3,4-dimethoxy-N,alpha-dimethyl-HCID 1223530892%

Reaction Conditions

Temperature4 °C

Reaction Steps

A solution of 15.1 g (78 mmol) of (3,4-dimethoxyphenyl) acetone (1) in 102 mL of methanol was cooled to 4° C. and was treated with 35 mL of 40% aqueous methylamine. To the reaction mixture, 3.5 g (92.5 mmol) of sodium borohydride was then added, and the temperature of the reaction was maintained at 4° C. The reaction mixture was allowed to stir for an additional 30 minutes, then concentrated under reduced pressure. To the residue, 60 mL of water was added, and the resulting reaction mixture was acidified to pH 1 using 6N HCl. The aqueous layer was extracted with 5×50 mL of dichloromethane, and the pH was adjusted to pH 13 using 6N NaOH. The aqueous layer was extracted with 4×75 mL of dichloromethane. The organic layers were combined, dried and concentrated to give 15 g (72 mmol, 92%) of 1A as a colorless oil (M+H, 210).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060847B2
Source datasetuspto-grants-2006_06
ORD IDord-887a460b861f40089b78e8cf5a4eb7bd
Source noteuspto-grants-2006_06