HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 13560729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-(1-Hydroxyhexyl)phenol | HCID 11790084 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Product | HCID 13560729 | HCID 13560729 | — |
| Product | 1-(3-Hydroxyphenyl)hexan-1-one | HCID 14349126 | — |
Reaction Steps
A solution of 1-(3-hydroxyphenyl)-1-hexanol (3 g) in methylene chloride (200 ml) was added to a well-stirred suspension of pyridinium chlorochromate (5.1 g) and sodium acetate (2.5 g) in methylenechloride (150 ml). The mixture was stirred at room temperature for two hours. Ether (100 ml) was added, and the brown granular preiipitate was removed by filtration. All volatiles were removed from the filtrate, and the residual liquid was purified by chromtography on silica gel using ether as eluent. The desired ketone, 3-hexanoylphenol, was isolated as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04794188 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-58b90a92d20b4fa4ac3e845e68d8004b |
| Source note | uspto-grants-1988_12 |