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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413164Generated: November 2, 2026

Formaldehyde → 3-[(dimethylamino)methyl]Benzenemethanol

https://huagongshe.com/reaction/2413164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant(3-BROMOBENZYL)DIMETHYLAMINEHCID 4341665—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product3-[(dimethylamino)methyl]BenzenemethanolHCID 1295201878%

Reaction Steps

3-Bromo-N,N-dimethylbenzylamine (21.4 g) was reacted with magnesium turnings (2.4 g) in dry tetrahydrofuran (75 ml). The mixture was cooled to 0° and gaseous formaldehyde (generated by heating 15 g paraformaldehyde in a stream of argon) was passed over the stirred solution. Tetrahydrofuran (25 ml) was added and the mixture was stirred at room temperature for 2.5 hours and acidified to pH 1. The mixture was extracted with aqueous 3N hydrochloric acid, and the aqueous extracts were made alkaline with aqueous sodium hydroxide and extracted with ether. The ether extracts were evaporated to give 3-(dimethylaminomethyl)benzyl alcohol (14.78 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496567
Source datasetuspto-grants-1985_01
ORD IDord-2d41ab2ae4414100b4679ce549b2957f
Source noteuspto-grants-1985_01