Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446711Generated: October 25, 2026

tert-Butyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylate → tert-Butyl 3-hydroxy-8-azabicyclo(3.2.1)octane-8-carboxylate

https://huagongshe.com/reaction/446711

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylateHCID 2794767—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-hydroxy-8-azabicyclo(3.2.1)octane-8-carboxylateHCID 2118772593.6%

Reaction Steps

3-Oxo-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (Compound 1009, 8 g, 35.5 mmol) was dissolved in 100 mL of ethanol. Sodium borohydride (2 g, 53.5 mmol) was added to the solution portionwise at room temperature. After stirring for 3 hours, the reaction was evaporated in vacuo to give clear viscous oil. The oil was dissolved in dichloromethane, washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated to afford 7.55 g of 3-hydroxy-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (Compound 1010) as a white crystalline solid; 1H NMR (300 MHz, DMSO-d6): δ 4.23 (dd, J=2.7, 4.6 Hz, 1H), 4.18-4.06 (m, 2H), 2.17-2.06 (m, 1H), 1.99-1.91 (m, 3H), 1.72-1.50 (m, 5H), 1.47 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481524B2
Source datasetuspto-grants-2013_07
ORD IDord-606c2d2fad3543d2b6d6a78e4aec908a
Source noteuspto-grants-2013_07