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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436477Generated: October 26, 2026

4-Methylmorpholine → (S)-2-Boc-amino-3-(3,5-difluorophenyl)propan-1-OL

https://huagongshe.com/reaction/1436477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant3,5-Difluoro-L-phenylalanine, N-BOC protectedHCID 2779009—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(S)-2-Boc-amino-3-(3,5-difluorophenyl)propan-1-OLHCID 5788101280%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Dissolve commercially available 2-(S)-tert-butoxycarbonylamino-3-(3,5-difluorophenyl)propionic acid (5.995 g, 19.9 mmol) in ethylene glycol dimethyl ether (20 mL) and cool −20° C. Add 4-methylmorpholine (2.4 mL, 21.89 mmol) and stir 5 min, then add isobutyl chloroformate (2.9 mL, 21.89 mmol) dropwise and stir 5 min. Filter into −15° C. cooled flask with course frit, rinse with cold ethylene glycol dimethyl ether. Add sodium borohydride (1.129 g, 29.85 mmol) in water (9 mL) followed by water (500 mL), then warm to room temperature. Filter and dissolve solid in dichloromethane. Wash with saturated aqueous sodium chloride, dry (magnesium sulfate) and concentrate to give the title compound as a solid (4.57 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618978B2
Source datasetuspto-grants-2009_11
ORD IDord-21d736e61fd143619af62201a24be08f
Source noteuspto-grants-2009_11