Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961548Generated: October 31, 2026

Ethyl Acetate → 3-[4-(Hydroxyimino-methyl)-phenyl]-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1961548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantHCID 21250649HCID 21250649—
SolventHexaneHCID 8058—
SolventWater ethanolHCID 19096565—
Product3-[4-(Hydroxyimino-methyl)-phenyl]-azetidine-1-carboxylic acid tert-butyl esterHCID 7666147994.51%

Reaction Steps

To a stirred suspension of 3-(4-Formyl-phenyl)-azetidine-1-carboxylic acid tert-butyl ester (Preparation 38, 6.5 g, 24.904 mmol, 1 equivalents) in ethanol:water (1:1, 120 mL) was added hydroxylamine hydrochloride (2.5 g, 37.356 mmol, 1.5 equivalents) followed by sodium acetate (3.67 g, 44.82 mol, 1.8 eq). Resulting reaction mixture was stirred at room temperature for 0.5 hours. Progress of the reaction was monitored by TLC using 20% ethyl acetate in hexane and visualized in UV light (254 nm). Reference of new spot and starting material was 0.32 and 0.67 respectively. After consumption of starting material, solvents was evaporated under reduced pressure and extracted with DCM (3×25 mL). Evaporation of volatiles provided light yellow solid (6.5 g, 94.51%). LC-MS and 1H NMR was consistent. 1H NMR (400 MHz, DMSO-d6) δ 1.39 (s, 9H), 3.81 (broad s, 3H), 4.42 (broad s, 2H), 7.36 (d, J=8 Hz, 2H), 7.57 (d, J=8 Hz, 2H), 8.12 (s, 1H), 11.19 (s, 1H). LC-MS (m/z):=277.30 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415310B2
Source datasetuspto-grants-2013_04
ORD IDord-d96e0417563441b2ae4f930a387c8743
Source noteuspto-grants-2013_04