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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10349Generated: October 25, 2026

Ethyl Acetate → 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/10349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium HydroxideHCID 14923—
ReactantBenzyl 2-methyl-1-oxa-5-azaspiro[2.4]heptane-5-carboxylateHCID 21041146—
SolventMethanolHCID 887—
Product3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl esterHCID 69068640—

Reaction Steps

A solution of 2-methyl-1-oxa-5-azaspiro[2,4]heptane-5-carboxylic acid benzyl ester (Example A9, 0.31 g, 1.25 mmol) in methanol (10 mL) and ammonium hydroxide (7 mL) is heated in a sealed tube at 100° C. for 16 hours. After cooling, the reaction mixture is dissolved ethyl acetate, washed with water, dried over Na2SO4 and evaporated to afford the title compound (0.340 g). 1H NMR (200 MHz, CDCl3): δ 7.33–7.26 (m, 5H), 5.28 (bs, 2H), 5.07 (s, 2H), 3.56–3.16 (m, 5H), 2.03–1.76 (m, 2H), 1.15 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094780B1
Source datasetuspto-grants-2006_08
ORD IDord-25d841ff62cf41b6862babb19ab9536f
Source noteuspto-grants-2006_08