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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377206Generated: October 30, 2026

(R)-beta-aminophenethyl alcohol → alpha-(Hydroxymethyl)benzylaminomethylpyrrolidine

https://huagongshe.com/reaction/377206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
Reactant(R)-tert-butyl 3-(((methylsulfonyl)oxy)methyl)pyrrolidine-1-carboxylateHCID 40479140—
SolventTolueneHCID 1140—
Productalpha-(Hydroxymethyl)benzylaminomethylpyrrolidineHCID 67654425126.8%

Reaction Steps

A solution of (R)-(-)-phenylglycinol (2.20 g, 16.1 mmol) and (3R)-N-tert-butyloxycarbonyl-3-methylsulphonyloxymethylpyrrolidine (Intermediate 1 part b; 1.0 g, 3.58 mmol), in toluene (20 ml), was heated at 150° C. for 6 h in a sealed pressure tube (Aldrich). The solvent was then removed under vacuum and the residue taken up into ethyl acetate (200 ml) and washed with water (×4). The organic was dried (MgSO4) and evaporated and the crude product chromatographed on silica gel eluting with CH2Cl2 /MeOH (97:3) to give the title-α-(hydroxymethyl) benzylaminomethylpyrrolidine (1.0 g, 87%), δ (360 MHz,CDCl3) 1.45 (9H, s, OC(Me)3), 1.52-2.60 (5H, m, CH2 and CH), 2.90-3.76 (7H, m, 3 of CH2 and CH), 7.25-7.39 (5H, m, Ar--H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025374
Source datasetuspto-grants-2000_02
ORD IDord-4865bf41034c45ca8c5dd6cd7d4b7d0d
Source noteuspto-grants-2000_02