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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746078Generated: November 1, 2026

Acryloyl chloride → HCID 69451735, compound

https://huagongshe.com/reaction/1746078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
ReactantSodium hydrideHCID 24758—
Reactant4-(2-Chlorophenyl)-3-hydroxy-1-(4-methoxyphenyl)azetidin-2-oneHCID 69446442—
SolventDichloromethaneHCID 6344—
ProductHCID 69451735HCID 6945173575.4%

Reaction Steps

To a solution of C3-hydroxy β-lactam 24 (5.80 g, 19.1 mmol) in 30 ml of freshly distilled CH2Cl2 was added NaH (60% suspension in mineral oil, 0.83 g, 21.0 mmol), and the mixture was stirred for 15 min at room temperature. Acryloyl chloride (2.59 g, 28.64 mmol) was then added dropwise and the resultant mixture was stirred until TLC indicated the disappearance of starting material. The reaction was quenched with a 5% solution of NH4Cl and extracted (3×20 ml) with CH2Cl2. The combined organic layers were dried over anhydrous MgSO4 and purified with column chromatography on silica gel (1:4, EtOAc:hexanes) to give 4.92 g (72%) of 25 as a white solid, mp 99-100° C. 1H NMR (250 MHz) δ 7.33 (d, J=7.9 Hz, 1H), 7.23-7.10 (m, 5H), 6.75 (d, J=8.9 Hz, 2H), 6.17 (d, J=5.0 Hz, 1H), 5.98 (dd, J=16.9, 1.00 Hz, 1H), 5.74 (dd, J=16.9, 10.4 Hz, 1H), 5.69 (d, J=5.0 Hz, 1H), 5.59 (d, J=10.4, 1.0 Hz, 1H), 3.66 (s, 3H). 13C NMR (63 MHz) δ 163.6, 161.2, 156.6, 133.7, 132.3, 130.3, 130.1, 129.8, 128.5, 126.8, 126.5, 118.6, 114.4, 75.3, 61.3, 58.2, 55.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149440B2
Source datasetuspto-grants-2015_10
ORD IDord-7ae16651f165450589a62bae60ec274e
Source noteuspto-grants-2015_10