HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095528Generated: October 31, 2026
4-Methylmorpholine → HCID 15043091, compound
https://huagongshe.com/reaction/2095528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 5-tert-Butyl N-((phenylmethoxy)carbonyl)-L-glutamate | HCID 107472 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15043091 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445674B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-24422c563835465f81ee152f79e006a8 |
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| Source note | uspto-grants-2013_05 |
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