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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504847Generated: October 30, 2026

Acetic Anhydride → Benzyl tert-butyl [3-(acetylamino)propane-1,2-diyl]biscarbamate

https://huagongshe.com/reaction/1504847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantBenzyl tert-butyl (3-aminopropane-1,2-diyl)biscarbamateHCID 86731716—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzyl tert-butyl [3-(acetylamino)propane-1,2-diyl]biscarbamateHCID 86731717—

Reaction Steps

To a solution of benzyl tert-butyl (3-aminopropane-1,2-diyl)biscarbamate (8.0 g, 25 mmol) and triethylamine (7.9 g, 78 mmol) in DCM (100 mL) was added acetic anhydride (2.8 g, 27 mmol) at 0° C. After 1 hour, the reaction mixture was diluted with ethyl acetate. The organic layer was concentrated under reduced pressure and the residue was purified by chromatography on silica gel to give benzyl tert-butyl [3-(acetylamino)propane-1,2-diyl]biscarbamate. MS ESI calc'd. for C18H28N3O5 [M+H]+ 366. found 366. 1H NMR (400 MHz, CD3OD) δ 7.34-7.30 (m, 5H), 5.01 (s, 2H), 3.59-3.51 (m, 3H), 2.87-2.77 (m, 2H), 2.0 (s, 3H), 1.42 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216173B2
Source datasetuspto-grants-2015_12
ORD IDord-f89a98cc85b543b18cb33b55f2b4f133
Source noteuspto-grants-2015_12