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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731375Generated: October 30, 2026

Sodium triacetoxyborohydride → HCID 57671211, compound

https://huagongshe.com/reaction/731375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57671198HCID 57671198—
SolventAcetic AcidHCID 176—
ProductHCID 57671211HCID 5767121128.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

2-Ethylamino-cyclopent-1-enecarboxylic acid ethyl ester (1.52 g, 8.30 mmol) was dissolved in glacial acetic acid (25 mL) and sodium triacetoxyborohydride (5.28 g, 24.9 mmol) was added at 0° C. The solution was allowed to warm to 25° C. and stirred for 3 h. The acetic acid was removed in vacuo and the residue was dissolved in dichloromethane. The solution was washed with saturated aqueous sodium bicarbonate solution followed by saturated aqueous brine solution. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo to afford the desired product, 2-ethylamino-cyclopentanecarboxylic acid ethyl ester (435.1 mg, 2.35 mmol, 28.3%), as a yellow oil. LC-MS (ESI) calcd for C10H19NO2 185.14, found 186.1 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-d1f5df01d64c465e8c568ce9df662649
Source noteuspto-grants-2009_09