HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenoxybenzoic acid → 3-Phenoxybenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenoxybenzoic acid | HCID 19539 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Product | 3-Phenoxybenzyl alcohol | HCID 26295 | — |
Reaction Steps
After filtering off the catalyst, the filtrate (reaction mixture), which consists of an organic phase containing the 3-phenoxy-benzaldehyde and an aqueous-alkaline phase containing the 3-phenoxy-benzoic acid is extracted with ether. After drying the combined ether extracts over sodium sulphate and stripping off the ether under nitrogen, 9.4 g of a residue which, according to analysis by gas chromatography, contains 96.9% of 3-phenoxy-benzaldehyde and 1.3% of still unreacted 3-phenoxy-benzyl alcohol remain. This gives a 3-phenoxy-benzyl alcohol conversion of 98.8%, a 3-phenoxy-benzaldehyde yield of 93% of theory and a selectivity for 3-phenoxy-benzaldehyde of 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04366325 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-1ac8ec003e9b4cc7bf650fc42b3aadcc |
| Source note | uspto-grants-1982_12 |