HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrophthalic anhydride → (Cyclohex-4-ene-1,2-diyl)dimethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrophthalic anhydride | HCID 6810 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Cyclohex-4-ene-1,2-diyl)dimethanol | HCID 325100 | 82% |
Reaction Steps
A solution of one hundred (100) parts by weight of a 1,2,3,6-tetrahydrophthalic anhydride in 500 parts of dry tetrahydrofuran is slowly added to a stirring mixture of 28.75 parts of lithium aluminum hydride and 162 parts of tetrahydrofuran. After the addition is complete, the mixture is refluxed for 24 hours. It is then hydrolyzed by a slow addition of a saturated Rochelle salt solution until it turns white. The mixture is refluxed for an additional 10 hours, allowed to room temperature, and suction filtered. The solvent is removed by a distillation and the viscous liquid crude product is purified by a fractional distillation under vacuum (yield 82%. b.p.: 165-170° C. at 12 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06454965B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-0544a4762f92461da53c36664d4a730a |
| Source note | uspto-grants-2002_09 |