HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237298Generated: October 30, 2026
Ethyl Acetate → 3-(2-Methoxy-benzyl)-azetidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/237298
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(2-Methoxy-benzoyl)-azetidine-1-carboxylic acid tert-butyl ester | HCID 58405054 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(2-Methoxy-benzyl)-azetidine-1-carboxylic acid tert-butyl ester | HCID 58405169 | 19% |
Reaction Steps
To a solution of 3-(2-methoxy-benzoyl)-azetidine-1-carboxylic acid tert-butyl ester (2.1 g, 7.2 mmol) in methanol (50 mL) was added sodium borohydride (1.08 g, 28.8 mmol). After stirring for 36 h, saturated sodium bicarbonate solution and EtOAc were added. The aqueous portion was extracted three times with EtOAc and the combined organic were dried (Na2SO4) and concentrated. To a solution of this material in ethanol (50 mL) was added 10% Pd/C. This reaction was then placed on a Parr hydrogenation apparatus with 60 psi of hydrogen gas. After 72 h, the reaction mixture was filtered through a pad of Celite and the filtrate concentrated. The crude product was purified by RP HPLC (basic conditions) to provide the title compound (370 mg, 19%). MS (ESI): mass calcd. for C16H23NO3, 277.2; m/z found, 222.2 [M-t-Bu]+. 1H NMR (CDCl3): 7.23-7.10 (m, 1H), 7.06 (d, J=7.3 Hz, 1H), 6.92-6.77 (m, 2H), 3.96 (t, J=8.0 Hz, 2H), 3.81 (s, 3H), 3.65-3.63 (m, 2H), 2.94-2.78 (m, 5H), 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-90e86f8526d74a42be236de4b4b8f0cd |
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| Source note | uspto-grants-2014_02 |
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