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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978704Generated: October 26, 2026

Hydrochloric Acid → [1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanol

https://huagongshe.com/reaction/978704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzylamineHCID 7504—
Reactant[3-(Bromomethyl)oxetan-3-yl]methanolHCID 529264—
SolventWaterHCID 962—
Product[1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanolHCID 20164320—

Reaction Conditions

Temperature100 °C

Reaction Steps

18.1 g of 1A and 11.7 g of benzylamine were mixed with 5 ml of water and the resulting mixture was stirred at 100° C. After 4 hours the solution was allowed to cool to ambient temperature and 13.8 ml of 36% (w/w) hydrochloric acid was added. The resulting mixture was stirred at 60° C. After 2 hours the solution was again allowed to cool to room temperature and then washed with dichloromethane to remove by-products. The aqueous layer was made alkaline by the addition of a solution of 5.5 g of sodium hydroxide in 10 ml of water and stirred at 100° C. for 1 hour. After cooling to ambient temperature the pH of the mixture was raised by addition of another solution of 5.5 g of sodium hydroxide in 10 ml of water and washed with hexane to remove benzylamine. The water was evaporated under reduced pressure, and the solid residue was taken up in dichloromethane. Inorganic salts, which remained undissolved, were removed by filtration, and the dichloromethane was evaporated in vacuo, leaving 1, as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665197
Source datasetuspto-grants-1987_05
ORD IDord-c4cd9b50b8c84c5e8537f76c629da15e
Source noteuspto-grants-1987_05