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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251471Generated: October 26, 2026

Benzyl chloroformate → Benzyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate

https://huagongshe.com/reaction/251471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant8-Azabicyclo(3.2.1)octan-3-oneHCID 434453—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylateHCID 1468253592.6%

Reaction Steps

8-azabicyclo[3.2.1]octan-3-one (5.10 g; 31.55 mmol) was dissolved in CH2Cl2 (50 mL) and treated with benzyl chloroformate (4.29 mL; 5.11 g; 29.98 mmol) DIPEA (16.48 mL; 12.23 g; 94.66 mmol) was added drop-wise (exothermic reaction). The resulting clear solution was allowed to stir at room temperature for 30 min and was subsequently diluted with 100 mL CH2Cl2. The organic phase was washed with 1 N HCl (2×100 mL), dried on Na2SO4 and concentrated to provide the crude product (7.2 g). 1H-NMR (400 MHz, CDCl3) δ 7.38 (m, 5H), 5.22 (s, 2H), 4.62 (s, 2H), 2.67 (m, 2H), 2.38 (d, J=15.9 Hz, 2H), 2.12 (m, 2H), 1.71 (dd, J=15.0, 7.2 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863449B2
Source datasetuspto-grants-2011_01
ORD IDord-a5c7a9263cd8484eb2811f0becd8a203
Source noteuspto-grants-2011_01