Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72410Generated: October 30, 2026

Acetic Acid → Tert-butyl 3-((4-fluoro-2-methylphenyl)(methyl)amino)azetidine-1-carboxylate

https://huagongshe.com/reaction/72410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 3-((4-fluoro-2-methylphenyl)amino)azetidine-1-carboxylateHCID 63303297—
Solvent1,2-DichloroethaneHCID 11—
ProductTert-butyl 3-((4-fluoro-2-methylphenyl)(methyl)amino)azetidine-1-carboxylateHCID 6795863867.5%

Reaction Steps

A solution of tert-butyl 3-((4-fluoro-2-methylphenyl)amino)azetidine-1-carboxylate (D30) (240 mg, 0.856 mmol), acetic acid (0.49 ml, 8.56 mmol), Formaldehyde 36% wt. in water (0.066 ml, 0.856 mmol) and sodium(triacetoxy)borohydride (725 mg, 3.424 mmol) in 1,2-dichloroethane (7 ml) was stirred under N2 atmosphere at room temperature for 1 day. NaHCO3 sat. solution (25 ml) was added. After phase separation, the aqueous layer was extracted with dichloromethane (2×35 ml). The organics after solvent evaporation were purified by Biotage SNAP-Si cartridge (10 g) eluting with cyclohexane/ethylacetate from 90/10 up to 80/20. Collected fractions after solvent evaporation afforded the title compound (D33) (170 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828987B2
Source datasetuspto-grants-2014_09
ORD IDord-00e345c050ee40bc899ad7ca1e38d891
Source noteuspto-grants-2014_09