Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Chloro-3-phenoxy-2-propanol | HCID 94300 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Catalyst | Chromium | HCID 23976 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Chloro-3-phenoxypropan-2-one | HCID 11622456 | 49.7% |
Reaction Steps
8N Jones reagent (100 ml.) was added dropwise to a stirred solution of 1-chloro-2-hydroxy-3-phenoxypropane (28.3 g.) in acetone (100 ml.) during 1 hour while maintaining the reaction temperature at 20° C. The mixture was then stirred for 4 hours, and then sufficient water was added to dissolve the precipitated chromium salts. The mixture was extracted three times with diethyl ether and the combined ethereal extracts were dried over sodium sulphate, concentrated under reduced pressure, dried again over sodium sulphate, and concentrated further and distilled, to give 1-chloro-3-phenoxyacetone (13.9 g.), b.p. 150°-155° C./20 mm.Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088695 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-aebca0dd54214c77b0232d4af4effbc5 |
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| Source note | uspto-grants-1978_05 |
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