HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → 1-(2-Chlorophenyl)-2-heptanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | 1-Nitropropane | HCID 7903 | — |
| Reactant | 1-Nitrohexane | HCID 12589 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Product | 1-(2-Chlorophenyl)-2-heptanone | HCID 15289939 | 17% |
Reaction Steps
Following a procedure similar to that described in Preparation 9, except that equivalent amounts of 2-chlorobenzaldehyde and nitrohexane were used in place of the 2-fluorobenzaldehyde and nitropropane, the title compound was obtained as a pale yellow oil in a yield of 17%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05288726 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-809ec52a031041cb93383a84c4655ebb |
| Source note | uspto-grants-1994_02 |