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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant3-azetidinecarboxylic AcidHCID 93192—
Reactant4-Bromo-3-fluorobenzaldehydeHCID 2783411—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethylorthoformateHCID 53629101—
SolventDichloromethaneHCID 6344—
ProductMethyl 1-(4-bromo-3-fluorobenzyl)azetidine-3-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080542B2
Source datasetuspto-grants-2011_12
ORD IDord-492108abe60e4a2989430bf04cfb827b
Source noteuspto-grants-2011_12