HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461131Generated: October 27, 2026
1,2-Dibromoethane → HCID 178443368, compound
https://huagongshe.com/reaction/1461131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 1-Bromo-3,7-dimethyloctane | HCID 137914 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178443368 | HCID 178443368 | — |
Reaction Steps
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, 50 ml of tetrahydrofuran and 3 droplets of ethylene dibromide in a similar manner to that described in Example 1 and cooled to 5° C., followed by the addition of 0.6 g (0.003 mol) of CuBr·(CH3)2S. The obtained mixture was stirred at that temperature for 30 minutes. 50 ml of a solution of 3.4 g (0.02 mol) of 3-chloro-6-methylene-2-methyloctadiene-1,7 having a purity of 70% in tetrahydrofuran was dropped into the resulting mixture over a period of 30 minutes. After the completion of the dropping, the obtained mixture was stirred at that temperature for one hour and subjected to TLC and HPLC to confirm the disappearance of the chlorine-containing raw material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05073659 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-339c2c3a8d8c4bacb9e01767cd2b4816 |
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| Source note | uspto-grants-1991_12 |
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