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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602086Generated: November 1, 2026

Methanol → (R)-beta-aminophenethyl alcohol

https://huagongshe.com/reaction/1602086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantPhenylglycine, D-HCID 70134—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
Product(R)-beta-aminophenethyl alcoholHCID 2724025—

Reaction Steps

20 g (920 mmol) of lithium borohydride are dissolved in 420 ml of absolute tetrahydrofuran. 233.5 ml (1.84 mol) of trimethylchlorosilane are added dropwise, while stirring, and 69.5 g (0.46 mol) of (R)-phenylglycine are then added in portions within the space of 4 hours. The reaction mixture is stirred at room temperature overnight. 690 ml of methanol are then added and the mixture is stirred at room temperature for 2 hours and concentrated in vacuo. The residue is dissolved, while stirring, in 690 ml of a 20% aqueous solution of potassium hydroxide. The aqueous phase is extracted three times with ethyl acetate. The combined organic phases are washed with water, dried over magnesium sulphate and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981492
Source datasetuspto-grants-1999_11
ORD IDord-62bef2d833174e03baf16a0eb74b762d
Source noteuspto-grants-1999_11