HuagongsheHuagongshe Chemistry Print Report · For research reference only
m,alpha-Dichlorotoluene → 5-(m-Chlorobenzyloxy)-2-pyridinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m,alpha-Dichlorotoluene | HCID 12103 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 6-(Hydroxymethyl)pyridin-3-ol hydrochloride | HCID 18758423 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(m-Chlorobenzyloxy)-2-pyridinemethanol | HCID 23467167 | — |
Reaction Steps
The solution of 16.2 g of 5-hydroxy-2-pyridinemethanol hydrochloride in 150 ml of methaol is added to a solution of 4.6 g of sodium in 250 ml of methanol, while stirring, over a period of 25 minutes. The solution is stirred for one hour and then a solution of 19.3 g of m-chlorobenzyl chloride in 50 ml of methanol is added. Then the mixture is refluxed for 19 hours, cooled, filtered and the filtrate evaporated to a residue. The residue is suspended in 100 ml of water, made basic with 20% aqueous sodium hydroxide solution and then extracted with chloroform. The chloroform extract is separated, dried over sodium sulfate, filtered and the filtrate evaporated, to yield 5-(m-chlorobenzyloxy)-2-pyridinemethanol melting at 78°-80°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260620 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-664c549644df454194d948c9d7af61de |
| Source note | uspto-grants-1981_04 |