Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21450269 | HCID 21450269 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21450281 | HCID 21450281 | — |
Reaction Steps
A well stirred mixture of 4-bromo-2-morpholino phenol (4.44g, 0.017 mole), benzyl chloride (2.3 ml, 0.02 mole), potassium carbonate (4.75g, 0.034 mole), and dry acetone (60 ml) was heated under reflux for 7 hours. The mixture was diluted with water, extracted with ether and the combined extracts washed with dilute sodium hydroxide solution and with water. Extraction of the ethereal solution with concentrated hydrochloric acid and evaporation of these extracts under reduced pressure gave 4-benzyloxy-3-morpholinobromobenzene hydrochloride, which was collected and washed with ether (5.29g, 80%, m.p. 164°-174° C). The hydrochloride, recrystallised from ethanol, had m.p. 168°-177° C. A suspension of the hydrochloride in water was treated with excess potassium carbonate and 4-benzyloxy-3-morpholinobromobenzene extracted into ether. Evaporation of the ether extracts gave the free base, m.p. 84°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011321 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-eed6c07b84fc457ab2aa465c2f748a92 |
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| Source note | uspto-grants-1977_03 |
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