HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608510Generated: November 2, 2026
4-Methylmorpholine → HCID 18659599, compound
https://huagongshe.com/reaction/1608510
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 15284423 | HCID 15284423 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18659599 | HCID 18659599 | — |
Reaction Steps
In 150 g of anhydrous THF were dissolved 5.4 g of N-benzyloxycarbonyl-L-leucyl-L-norleucine prepared in the same manner as in Example 1-(b) and 3.4 ml of N-methylmorpholine, and 1.6 g of ethyl chloroformate was added thereto under ice-cooling, followed by stirring at 0° C. for 30 minutes. The reaction mixture was added to an excess diazomethane solution in diethyl ether, and the solution was allowed to stand at 0° C. for 1 hour. The solvent was removed by distillation under reduced pressure, and the residue was purified by medium-pressure column chromatography on silica gel to obtain 4.0 g of the titled compound as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05395824 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-05280ccf94194cc7b10f471d585a4ca8 |
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| Source note | uspto-grants-1995_03 |
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