Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-1-hexanol | HCID 77970 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Morpholinehexanol | HCID 22218504 | 98.9% |
Reaction Steps
A suspension of morpholine (3.30 mL, 3.30 g, 37.8 mmol), 6-bromo-1-hexanol (6.72 g, 72.3 mmol), ethanol (20 mL), and potassium carbonate (6.23 g, 45.1 mmol) was stirred for 36 hours at 25° C., after a slight exotherm at the beginning. The reaction mixture was diluted with ethyl acetate (30 mL), filtered and concentrated. The residue was taken up in ethyl acetate, filtered and concentrated. The 7.0 g of 4-(6-hydroxyhexyl)morpholine was isolated as a yellow oil and used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700775B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-37690b49f28f4a21958d402ccc1b59d7 |
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| Source note | uspto-grants-2010_04 |
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