HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bromide → HCID 13635748, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | 1-Cyclohexene-1-butanol, .gamma.-methyl- | HCID 66584171 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13635748 | HCID 13635748 | 66% |
Reaction Steps
NaBr (0.6 g, 0.006 mol) and NaHCO3 (6.4 g, 0.076 mol) were mixed together with water (60 ml), toluene (250 g) and 4-(cyclohex-1-en-1-yl)-3-methyl butan-1-ol (96 g (0.573 mol, purity: 99% sum of the isomers) at room temperature with continuous stirring. NaOCl (13% w/w aqueous 426.8 g, 0.745 mol) was added to the reaction mass over 2 h. Stirring was continued for another 1 h. The aqueous phase was removed, organic phase was washed with a solution of NaHCO3 and then with water. The organic phase thus obtained was concentrated and crude product purified by fractional distillation to provide 4-(cyclohex-1-en-1-yl)-3-methylbutanal (62.6 g, yield: 66%, GC purity: 95% sum of the isomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187709B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-5cd1db1362bd4ace8a2d30577b0d3b2b |
| Source note | uspto-grants-2015_11 |