HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Chloro-o-xylene → HCID 12884120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Chloro-o-xylene | HCID 11093 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2,5,5-Trimethyl-tetrahydro-furan-2-yl)-methanol | HCID 12634236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12884120 | HCID 12884120 | 80% |
Reaction Steps
2,5,5-Trimethyl-2-hydroxymethyl tetrahydrofuran (1.6 g) was added slowly to a stirred suspension of sodium hydride (0.4 g of 80% dispersion in oil) in dry toluene (55 ml). After the addition the mixture was heated under reflux for 1 hour. 2-Methylbenzyl chloride (1.8 g) was added and the mixture heated under reflux overnight. The cooled mixture was washed with water (x2) and dried and the solvent was removed under reduced pressure. The product was purified by chromatography on silica using methylene dichloride as eluent. Yield 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE030574 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-31a0d20491b14ed286272cdd3e4cf655 |
| Source note | uspto-grants-1981_04 |