HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 14303120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 14303131 | HCID 14303131 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14303120 | HCID 14303120 | 86.6% |
Reaction Steps
60 g (0.37 mol) of N-bromosuccinimide are added in portions to 88.8 g (0.3 mol) of 6-(4-chloro-3-methylphenoxy)-5-hydroxy-5,6,6-trimethyl-1-hexene in 600 ml of absolute chloroform, while stirring and cooling, so that the reaction temperature does not exceed 40° C. When the addition has ended, the mixture is stirred at room temperature for a further 14 hours and then washed twice with water and dried over sodium sulphate and the solvent is removed in vacuo. 94 g (82% of theory) of 2-bromomethyl-5-[2-(4-chloro-3-methylphenoxy)-prop-2-yl]-5-methyl-tetrahydrofuran are obtained and are further reacted without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04826836 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-bc6a87ea02254d82bb52f99a5e2e74ab |
| Source note | uspto-grants-1989_05 |