Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934381Generated: October 31, 2026

Ethanol → (R)-1-[3-(1-tert-butoxycarbonyl-4-piperidyl)-(E)-acryloyl]-3-piperidinecarboxylic acid

https://huagongshe.com/reaction/1934381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantLithium HydroxideHCID 3939—
Reactantethyl (R)-1-[3-(1-tert-butoxycarbonyl-4-piperidyl)-(E)-acryloyl]-3-piperidinecarboxylateHCID 86758023—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-1-[3-(1-tert-butoxycarbonyl-4-piperidyl)-(E)-acryloyl]-3-piperidinecarboxylic acidHCID 6981799074.1%

Reaction Steps

A solution of LiOH (0.32 g) in H2O (20 ml) was added to a solution of ethyl (R)-1-[3-(1-tert-butoxycarbonyl-4-piperidyl)-(E)-acryloyl]-3-piperidinecarboxylate (4.46 g) in tetrahydrofuran (20 ml)-EtOH (20 ml) at 0° C. The reaction mixture was stirred for 3 hours at the same condition, and the solvent was evaporated in vacuo. The residue was resolved in ethyl acetate-water, and acidified with 10% aq. KHSO4. The whole was washed with water, brine, dried over MgSO4, and evaporated in vacuo, subsequently. The residue was recrystallized from diethyl ether to give (R)-1-[3-(1-tert-butoxycarbonyl-4-piperidyl)-(E)-acryloyl]-3-piperidinecarboxylic acid as a white solid (3.07 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384028B1
Source datasetuspto-grants-2002_05
ORD IDord-e4a155b003454d9f9708f32ecab8adce
Source noteuspto-grants-2002_05