HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764776Generated: October 26, 2026
4-Methylmorpholine → HCID 124669052, compound
https://huagongshe.com/reaction/1764776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | L-Glutamic acid, 5-(phenylmethyl) ester | HCID 122337 | — |
| Reactant | Boc-Ala-OSu | HCID 11011585 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 124669052 | HCID 124669052 | — |
Reaction Steps
H-Glu(OBzl)-OH (7.0 g, 29.5 mmol) was finely ground in a mortar and pestle and then stirred with 8.88 g (32.3 mmol) of Boc-Ala-OSu for 48 hours in 250 ml DMF in the presence of 6 ml N-methylmorpholine (NMM). Some more NMM was added to maintain the reaction slightly basic during the reaction. The solvent was evaporated and the residue partitioned between 30 ml ethyl acetate and 500 ml H2O containing 2 ml of 10% H2SO4. The organic layer was then washed three times with water, dried(Na2SO4) and evaporated to dryness. The product was taken up in a small volume of ether and treated with a large volume of petroleum ether. A white amorphous solid was obtained which was homogeneous on tlc: Yield, 11.0 g (91.5%); mp 84°-88°; [α]D25 = -8.08° (c l, DMF).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04116951 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-4b00c66b007f4e359d101c294560c3b3 |
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| Source note | uspto-grants-1978_09 |
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