HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → HCID 178443368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 1-Bromo-3,7-dimethyloctane | HCID 137914 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 6-Chloro-7-methylene-3-methyl-1-octen-3-yl acetate | HCID 11160593 | — |
| Reactant | HCID 178443371 | HCID 178443371 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178443368 | HCID 178443368 | — |
Reaction Steps
In a similar manner to that described in Example 1, a tetrahydrofuran solution of 3,7-dimethyloctylmagnesium bromide was prepared from 6.64 g (0.03 mol) of 3,7-dimethyloctyl bromide, 0.73 g of metallic magnesium, 40 ml of tetrahydrofuran and 3 droplets of ethylene bromide and converted into a tetrahydrofuran solution of 3,7-dimethyloctylzinc chloride by the addition of 4.08 g (0.03 mol) of anhydrous zinc chloride. The subsequent step was conducted with this solution, 0.2 g (0.001 mol) of CuBr·(CH3)2S and 4.4 g (0.02 mol) of 6-chloro-7-methylene-3-methyl-1-octen-3-yl acetate in a similar manner to that described in Example 20 to give 4.1 g of the objective compound as a colorless liquid (yield: 61.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05073659 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-de217d34892e4e7e9c4ee530ba481659 |
| Source note | uspto-grants-1991_12 |