HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435153Generated: October 31, 2026
Acetic Acid → 3-[(2,4-Dichlorobenzylamino)-methyl]-azetidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1435153
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2,4-Dichlorobenzaldehyde | HCID 13404 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Tert-butyl 3-(aminomethyl)azetidine-1-carboxylate | HCID 10679125 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-[(2,4-Dichlorobenzylamino)-methyl]-azetidine-1-carboxylic acid tert-butyl ester | HCID 69002977 | 65.2% |
Reaction Steps
To a solution of 3-aminomethyl-azetidine-1-carboxylic acid tert-butyl ester (300 mg, 1.6 mmol), 2,4-dichlorobenzaldehyde (281 mg, 1.61 mmol) and acetic acid (0.09 mL, 1.61 mmol) in 1,2-dichloroethane (16 mL) at 0° C. is added sodium triacetoxy-borohydride (476 mg, 2.25 mmol). The reaction is warmed to ambient temperature and stirred overnight under N2. The reaction mixture is poured on to 2N NaOH (20 mL) and extracted with ethyl acetate (3×). The combined organic extracts are washed with aqueous saturated NaCl, dried (Na2SO4), filtered and concentrated. The crude product is purified by flash chromatography on silica gel eluting with 5% EtOH (10% NH4OH)/chloroform to yield 360 mg (65%) of 3-[(2,4-dichlorobenzylamino)-methyl]-azetidine-1-carboxylic acid tert-butyl ester. 1H NMR (400 MHz, CD3OD) δH: 7.49-7.47 (2H, m), 7.36-7.34 (1H, m), 4.05-4.01 (2H, m), 3.88 (2H, s), 3.64-3.61 (2H, m), 2.8 (2H, m), 2.78-2.74 (1H, m), 1.46 (9H, s). Mass spectrum (ion spray): m/z=345.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07615648B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-909bc2b191724333b1458f9363f4df5b |
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| Source note | uspto-grants-2009_11 |
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