HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658980Generated: October 29, 2026
Acetic Acid → Methyl 1-(4-bromo-3-fluorobenzyl)azetidine-3-carboxylate
https://huagongshe.com/reaction/658980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-azetidinecarboxylic Acid | HCID 93192 | — |
| Reactant | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 1-(4-bromo-3-fluorobenzyl)azetidine-3-carboxylate | HCID 59651823 | — |
Reaction Steps
Azetidine-3-carboxylic acid (43 g, 421 mmol), 4-bromo-3-fluorobenzaldehyde (81.4 g, 401 mmol), methyl orthoformate (219 mL, 2005 mmol), and AcOH (34 mL, 601 mmol) were added to DCM (700 mL) at rt under an N2 atmosphere. The mixture was stirred for 15 min, at which point sodium triacetoxyborohydride (127 g, 601 mmol) was added portion-wise (exothermic). After 2 h, solvent swap with MeOH (257 g, 8019 mmol), and sulfuric acid (79 g, 802 mmol) was added slowly (exothermic). The mixture was heated at reflux for 18 h. Solvent was removed and the mixture was extracted using DCM and water. The organic layer was purified using a Biotage column (isopropanol/heptane), affording methyl 1-(4-bromo-3-fluorobenzyl)azetidine-3-carboxylate as a clear oil. MS (ESI) m/z: Calculated: 301.0; Observed: 302.0 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080542B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-492108abe60e4a2989430bf04cfb827b |
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| Source note | uspto-grants-2011_12 |
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