HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656096Generated: October 27, 2026
Tetrahydrofuran → morpholine 5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide
https://huagongshe.com/reaction/1656096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Acetylmorpholine | HCID 15543 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Methyl-2-benzyloxyphenyl propiolate | HCID 54058410 | — |
| Solvent | Water | HCID 962 | — |
| Product | morpholine 5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide | HCID 86747286 | 61% |
Reaction Steps
Acetyl morpholine (546 ul, 4.72 mmole) was dissolved in 10 ml dry tetrahydrofuran in an oven dried 50 ml two neck round bottom flask under nitrogen. The solution was cooled to 0° C. and was treated slowly dropwise with lithium diisopropylamide (3.2 ml, 4.72 mmole). The mixture was stirred 30 minutes at 0° C. and was treated with methyl-2-benzyloxyphenyl propiolate (600 mg, 2.25 mmole) in 2 ml dry tetrahydrofuran. The reaction mixture was stirred for 1 hour at 0° C. and was diluted with 10 ml water. The volatiles were removed in vacuo and the residue was crystallized from diethyl ether/methanol (20:1). The tan solid was collected, was washed with diethyl ether, and was dried to afford 500 mg (61%) of morpholine-5-(2-Benzyloxyphenyl)-3-oxo-pent-4-ynamide as a tan solid. Melting Point: 224°-227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05252735 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-c4388469e9584938a636f53fdfa3d980 |
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| Source note | uspto-grants-1993_10 |
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