HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenoxybenzoic acid → o-Phenoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenoxybenzoic acid | HCID 75237 | — |
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | 2-Phenoxybenzyl alcohol | HCID 3660111 | — |
| Reactant | lithium aluminium hydride THF | HCID 68718528 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | o-Phenoxybenzaldehyde | HCID 88060 | 78% |
Reaction Steps
A mixture of 2-phenoxybenzyl alcohol (4.0 g, 20.2 mmol, prepared by the reduction of commercially available 2-phenoxybenzoic acid with LiAlH4 /THF) and 150 mL CH2Cl2 was treated with pyridinium dichromate (11.39 g, 30.3 mmol) at 25° C. and stirred for another 36 hours. The mixture was filtered through d.e. and then through a pad of silica gel to produce 3.11 g (78%) of title compound as a yellow oil. 1H NMR (CDCl3) δ6.8 (d, 1H), 6.9 (d, 1H), 7.0 (m, 2H), 7.1 (m, 2H), 7.2 (m, 1H), 8.9 (m, 1H), 10.2 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721255 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-404ef53e5420495e896d2796b7bf052d |
| Source note | uspto-grants-1998_02 |