HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dibromoethane → 2,3-Dihydro-1,4-benzodioxine-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,3-Dihydroxybenzaldehyde | HCID 90579 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3-Dihydro-1,4-benzodioxine-5-carbaldehyde | HCID 2795033 | 70% |
Reaction Steps
2,3-Dihydroxybenzaldehyde (58 g, 420 mmol) was added to a refluxing mixture of dibromoethane (107.4 g, 570 mmol), sodium hydroxide (35.7 g, 890 mmol) and tetrabutyl ammonium bromide (3 g) in water (50 mL). After heating at reflux for 4 h, the mixture was cooled and the organic layer separated, washed with base, dried over sodium sulfate and concentrated in vacuo. The residue was Kugelrohr distilled at 135° to give the product (48 g, 70%) which solidified on standing (mp 61-62° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06060506 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-75172d31cca94ca4a50716e2551e37bb |
| Source note | uspto-grants-2000_05 |