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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095528Generated: October 31, 2026

4-Methylmorpholine → HCID 15043091, compound

https://huagongshe.com/reaction/2095528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
Reactant5-tert-Butyl N-((phenylmethoxy)carbonyl)-L-glutamateHCID 107472—
ReactantPotassium bisulfateHCID 516920—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15043091HCID 15043091—

Reaction Steps

In analogy to G. Kokotos (Synthesis 1990, 299), a solution of 5.00 g (14.8 mmol) of Z-Glu(OtBu)-OH in 74.0 ml of THF was treated at −10° C. with 1.63 ml (14.8 mmol) of 4-methylmorpholine, 1.41 ml (14.8 mmol) of ethyl chloroformate. After 10 min 1.682 g (44.5 mmol) of natriumborohydrid was added in one portion. Methanol (148 ml) was then added dropwise over a period of 25 min at 0° C. The solution was stirred 20 min, and then neutralized with a 10% KHSO4 solution. The organic solvents are evaporated under reduced pressure and the obtained residue is poured on a 10% KHSO4 extracted with EtOAc (3×). The organic phases were washed with aqueous 10% KHSO4, 10% NaCl, dried over Na2SO4 and evaporated to yield 5.16 g (quantitative) of the titled compound as yellow oil. MS: 324.18 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445674B2
Source datasetuspto-grants-2013_05
ORD IDord-24422c563835465f81ee152f79e006a8
Source noteuspto-grants-2013_05