HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 9838153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | 1-Ethoxy-2,3-Difluorobenzene | HCID 2782928 | — |
| Reactant | HCID 178506865 | HCID 178506865 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 9838153 | HCID 9838153 | — |
Reaction Steps
1.1 kg/h of a 1 M solution of 2,3-difluorophenetole containing 10 mol % of 2,2,6,6-tetramethylpiperidine were introduced into a continuous-flow reactor and mixed with 0.4 kg/h of a 2.5 M solution of hexyllithium in hexane at −35° C. After the mixture had passed through the reaction zone, 0.28 kg/h of a 4.7 M solution of benzaldehyde in THF was mixed in. After the reaction had finished, the product was collected and worked up in the customary manner, giving 2,3-difluoro-4-ethoxy-α-phenylbenzyl alcohol. The conversion based on the starting compound was 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207835B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-2c79ef8fe2e94c688b9316149898a8f1 |
| Source note | uspto-grants-2001_03 |