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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588797Generated: October 30, 2026

Acetic Acid → tert-Butyl 3-(3-(acrylamido)azetidin-1-yl)azetidine-1-carboxylate

https://huagongshe.com/reaction/588797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTriethylamineHCID 8471—
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(azetidin-3-yl)acrylamide hydrochlorideHCID 131734447—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-(3-(acrylamido)azetidin-1-yl)azetidine-1-carboxylateHCID 9046270131.4%

Reaction Steps

To a mixture of N-(azetidin-3-yl)acrylamide hydrochloride (500 mg, 3.40 mmol), tert-butyl 3-oxoazetidine-1-carboxylate (684 mg, 4.0 mmol), Et3N (343 mg, 3.40 mmol) and AcOH (100 mg, 0.167 mmol) in DCM (20 mL), NaBH(OAc)3 (2.16 g, 10.2 mmol) was added, and the resulting mixture was stirred at room temperature for 16 h. The mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated NaHCO3 solution and brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (DCM/MeOH=100:1 to 20:1) to afford the desired product (300 mg, 31% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227978B2
Source datasetuspto-grants-2016_01
ORD IDord-e9802b4dc8954c3b8a8cb1df8bb1e09b
Source noteuspto-grants-2016_01