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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383726Generated: November 2, 2026

4-Methylmorpholine → HCID 131722742, compound

https://huagongshe.com/reaction/1383726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 86757100HCID 86757100—
SolventDimethylformamideHCID 6228—
ProductHCID 131722742HCID 131722742—

Reaction Steps

To a solution of 492 mg (1.51 mmol) of N-[bis-(methyl-thio)methylene]-3-t-butylphenylalanine in 5 ml of DMF, 0.183 ml (1.66 mmol) of NMM and 0.159 ml (1.66 mmol) of ethyl chloroformate were added at −15° C. and the mixture was stirred for 30 minutes. The reaction mixture was stirred with bubbling of ammonia gas for another 30 minutes, left to stand at room temperature, diluted with ethyl acetate and washed first with water, then with saturated brine. The organic layer was dried with anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure; the resulting residue was dissolved in 3 ml of 1,4-dioxane and, after adding 1 ml of 2 N hydrochloric acid, the solution was stirred at room temperature for 3 days. Under cooling with ice, the solution was neutralized with saturated aqueous NaHCO3, extracted with chloroform, and washed first with water, then with saturated brine. The organic layer was dried with magnesium sulfate and concentrated under reduced pressure; the resulting residue was subjected to silica gel column chromatography (eluting solvent; chloroform:methanol=10:1) to give Phe(3-tBu)-NH2 in the amount of 210 mg (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255285B1
Source datasetuspto-grants-2001_07
ORD IDord-83317e49e1864bac90ed1fef3818e153
Source noteuspto-grants-2001_07