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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467512Generated: November 1, 2026

Methylamine → HCID 12027889, compound

https://huagongshe.com/reaction/1467512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-(Diethoxymethyl)benzaldehydeHCID 595993—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 12027889HCID 1202788998.5%

Reaction Steps

A mixture of 4-(diethoxymethyl)benzaldehyde (1.04 g, 5 mmol) and methylamine (27˜32% solution in methanol, 2.3 g, 20 mmol) in methanol (20 mL) was stirred at room temperature for 40 mins. The mixture was cooled to 0° C., sodium borohydride (0.284 g, 7.5 mmol) was added portionwise. After the addition, the mixture was stirred at room temperature for 4 hr. Methanol was removed under reduced pressure. The residue was partitioned between water (50 mL) and ethyl acetate (50 mL). The organic layer was separated. The aqueous layer was extracted with ethyl acetate (50 mL×3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and concentrated to give crude 1-(4-(diethoxymethyl)phenyl)-N-methylmethanamine (1.1 g) as a light yellow oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999987B2
Source datasetuspto-grants-2015_04
ORD IDord-c8b4a32600284fbc96b323ce1a3e3908
Source noteuspto-grants-2015_04