HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 767785, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1-(4-Phenylcyclohexyl)ethanone | HCID 12883749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 767785 | HCID 767785 | 46% |
Reaction Steps
To a suspension of AlCl3 (5.9 g, 54 mmol) in DCM (200 mL) at 0° C. was added 1-(4-phenylcyclohexyl)ethanone (9 g in DCM), and acetyl chloride (10.4 mL, 146 mmol) dropwise over 30 min. The mixture was stirred to rt for 15 min. and heated at 45° C. for 4 h. After being cooled to rt, the mixture was poured it into ice-HCl (1N). The organic layer was collected, and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were combined, concentrated and purified on column (hexane:ethyl acetate, 8:2) to give 1-(4-(4-acetylcyclohexyl)phenyl)ethanone (A2) as a mixture of two isomers (5 g, 46% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120779B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-5aacef1781a341468d9033786605ddd6 |
| Source note | uspto-grants-2015_09 |