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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403276Generated: October 29, 2026

Triethylamine → HCID 67475266, compound

https://huagongshe.com/reaction/403276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 2-oxoazetidine-1-carboxylateHCID 23179885—
ReactantHCID 67287646HCID 67287646—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
ProductHCID 67475266HCID 6747526684%

Reaction Steps

To a solution of compound 1d (diHCl salt, 2.7 g, 10 mmol) and N-Boc azetidinone 1e (2.4 g, 14 mmol) in 1,2-DCE (50 mL) was added slowly Et3N (20 mmol) followed by acetic acid (3.5 mL). To this mixture was added Na(OAc)3BH (3.39 g, 16 mmol). The reaction was stirred at room temperature for 5 h. To the reaction mixture was added aq. NaHCO3, and the resultant mixture was extracted with CH2Cl2. The organic layer was dried over Na2SO4 and concentrated. Purification by flash column chromatography (silica gel, 80% EtOAc/heptane) gave compound 1f (2.96 g). 1H NMR (300 MHz, CDCl3): δ 7.91 (m, 1H), 7.53 (m, 1H), 4.28 (m, 1H), 4.22-4.11 (m, 2.5; H), 3.91 (m, 0.5; H), 3.83 (m, 1H), 3.73-3.60 (m, 3.5; H), 3.49 (m, 0.5; H), 3.41 (m, 1H), 2.11 (m, 1H), 1.89-1.73 (m, 1H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748417B2
Source datasetuspto-grants-2014_06
ORD IDord-b361746539a94224bbf393d0020bf052
Source noteuspto-grants-2014_06