HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613615Generated: October 30, 2026
N-Formylmorpholine → HCID 15322096, compound
https://huagongshe.com/reaction/1613615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Formylmorpholine | HCID 20417 | — |
| Reactant | 7-Bromo-2,3,4,5-tetrahydro-1-benzoxepin-5-ol | HCID 19774223 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15322096 | HCID 15322096 | 105.9% |
Reaction Steps
254 ml (0.6 mole) of a 1.7 molar solution of tert.-butyllithium in n-pentane is slowly added dropwise under argon to a stirred solution of 48.6 g (0.2 mole) of 7-bromo-5-hydroxy-2,3,4,5-tetrahydro-1-benzoxepin in 550 ml of absolute THF at -90° C. to -100° C. The mixture is subsequently stirred at -78° C. for 1 hour and then, at this temperature, a solution of 24 ml (0.24 mole) of N-formylmorpholine in 180 ml of absolute THF is added dropwise while stirring vigorously. The mixture is stirred at -78° C. for 1 hour and subsequently allowed to warm to 0° C., and is diluted with diethyl ether and hydrolyzed with ice-water. After extraction several times with diethyl ether, the combined organic extracts are washed with water and saturated brine and dried over sodium sulfate, and the solvent is stripped off in vacuo. 40.7 g of yellowish oil are obtained and reacted further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05194442 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-d5a944520e0e42d0afacac9095d10382 |
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| Source note | uspto-grants-1993_03 |
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