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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731370Generated: October 30, 2026

Ethyl 2-oxocyclopentanecarboxylate → HCID 12813948, compound

https://huagongshe.com/reaction/731370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethylamine hydrochlorideHCID 6364545—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 12813948HCID 12813948—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-oxo-cyclopentanecarboxylic acid ethyl ester (3.00 g, 19.2 mmol) in ethanol (20 mL) was treated with methylamine hydrochloride (1.296 g, 19.2 mmol), sodium cyanoborohydride (2.42 g, 38.4 mmol), and glacial acetic acid (10 drops) and stirred for 16 h at 50° C. After cooling to 25° C. the solvent was removed in vacuo, the crude material was redissolved in ethyl acetate (100 mL) and washed with saturated aqueous sodium bicarbonate solution (100 mL). The aqueous layer was discarded and the organic layer was washed with 1.0 M aqueous hydrochloric acid solution (50 mL). The organic layer was discarded, 1.0 M aqueous sodium hydroxide solution (75 mL) was added and the aqueous layer was extracted with ethyl acetate (100 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was removed in vacuo to afford the crude product, 2-methylamino-cyclopent-1-enecarboxylic acid ethyl ester, as a light yellow oil. LC-MS (ESI) calcd for C9H15NO2 169.11, found 170.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-a96594af30df47d98199fab1f53d33c6
Source noteuspto-grants-2009_09