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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | tert-Butyl 3-(methoxy(methyl)carbamoyl)azetidine-1-carboxylate | HCID 21306970 | — |
| Reactant | HCID 178489560 | HCID 178489560 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(2-Methoxy-benzoyl)-azetidine-1-carboxylic acid tert-butyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642583B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7e2371a239da41baa24014c01d9a06dc |
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| Source note | uspto-grants-2014_02 |
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