HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → Cyclohexanecarbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Product | Cyclohexanecarbonyl chloride | HCID 75938 | — |
Reaction Steps
Compound of formula (XI) where all R5s are H and R7 and R8 are methyl was prepared by reacting 4-PgO benzoic acid chloride, prepared as in the above paragraph, in a Grignard reaction with CH3MgCl in a procedure similar that employed in Example I for producing (1-methyl-l-hydroxy) ethyl-3-cyclohexene from 3-cyclohexane carboxylic acid chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06197122B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-f9db31b1eab54f7b961fcb5a525c682d |
| Source note | uspto-grants-2001_03 |