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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237297Generated: October 25, 2026

Ethyl Acetate → 3-(2-Methoxy-benzoyl)-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/237297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium bisulfateHCID 516920—
Reactanttert-Butyl 3-(methoxy(methyl)carbamoyl)azetidine-1-carboxylateHCID 21306970—
ReactantHCID 178489560HCID 178489560—
SolventDiethyl EtherHCID 3283—
Product3-(2-Methoxy-benzoyl)-azetidine-1-carboxylic acid tert-butyl esterHCID 58405054—

Reaction Steps

To a solution of 3-(methoxy-methyl-carbamoyl)-azetidine-1-carboxylic acid tert-butyl ester (3.48 g, 14.2 mmol) in dry ether (150 mL) at 0° C. was added 2-methoxylphenylmagnesium bromide (1.0 M in THF, 17 mL, 17 mmol). The reaction was allowed to slowly warm to rt and stirred for 36 h. Then a solution of 1M KHSO4 and EtOAc were added and the aqueous portion was extracted once with EtOAc. The combined organic fractions were dried (Na2SO4) and concentrated to provide the title compound. This material was used in subsequent reactions without additional purifications. MS (ESI): mass calcd. for C16H21NO4, 291.1; m/z found, 236.1 [M-t-Bu]+. 1H NMR (CDCl3): 7.83 (dd, J=7.8, 1.8 Hz, 1H), 7.51 (ddd, J=8.5, 7.3, 1.8 Hz, 1H), 7.06-6.95 (m, 2H), 4.13-4.03 (m, 5H), 3.90 (s, 3H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642583B2
Source datasetuspto-grants-2014_02
ORD IDord-7e2371a239da41baa24014c01d9a06dc
Source noteuspto-grants-2014_02