HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2,2,2-Trichloro-1-phenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | 3-Nitro-alpha-(trichloromethyl)benzenemethanol | HCID 2725814 | — |
| Product | 2,2,2-Trichloro-1-phenylethanol | HCID 16150 | — |
| Product | 2,2,2-Trichloro-1-(4-methoxyphenyl)ethan-1-ol | HCID 5177931 | — |
Reaction Steps
Following the procedure of Example I and substituting benzaldehyde, 4-anisaldehyde and other starting material compounds and substituting the reagents of Example II, there is obtained trichloromethylbenzyl alcohol, trichloromethyl-4-methoxybenzyl alcohol and the benzaldehyde corresponding to said starting material compound, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04603227 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-c4adb5a068ea450888597dbb92e82d82 |
| Source note | uspto-grants-1986_07 |