HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-Phenoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | 3-Phenoxybenzaldehyde | HCID 38284 | 95.5% |
| Product | Bisulfite | HCID 104748 | — |
Reaction Steps
A solution of 200 g of sodium metabisulfite in 800 ml of water was added to a solution of 200 g of m-phenoxy-benzaldehyde in 800 ml of isopropyl ether and after the addition of 250 ml of methanol, the mixture was stirred for 3 hours and was vacuum filtered. The recovered precipitate was washed with 1--1 water-methanol mixture and then with isopropyl ether and was dried to obtain 295 g of the combination bisulfite of m-phenoxy-benzaldehyde (titer of 95.5% mobile hydrogen). The product was crystallized from 4 volumes of ethyl acetate to obtain a 97.6% yield of the product with a titer of mobile hydrogen of 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04202835 |
| Source dataset | uspto-grants-1980_05 |
| ORD ID | ord-141b17c4d9984fa78d56506b6063d7ed |
| Source note | uspto-grants-1980_05 |