HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654947Generated: October 30, 2026
1,2-Dibromoethane → HCID 19885932, compound
https://huagongshe.com/reaction/654947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
| Reactant | HCID 21705970 | HCID 21705970 | — |
| Reactant | HCID 178419678 | HCID 178419678 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19885932 | HCID 19885932 | — |
Reaction Steps
To a stirred solution of 8-(thiophene-2-yl)octyl magnesium bromide [0.62 mmol, prepared from 1-bromo-8-(thiophen-2-yl)octane; 0.170 g, 0.620 mmol and 1.24 mmol magnesium with a catalytic amount of 1,2 dibromoethane as initiator] in tetrahydrofuran (2 ml) at 0° under argon was added dropwise 5-trimethylsilyl-3-furaldehyde (0.104 g, 0.620 mmol) in tetrahydrofuran (3 ml). The solution was warmed to room temperature, stirred for one hour, quenched with saturated ammonium chloride solution and extracted into ethyl ether. The organic portion was washed with saturated sodium bicarbonate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to a yellow oil. Purification by flash chromatography (silica, 5 to 10% ethyl acetate/hexane) gave the desired alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134128 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-52607143f4244f858675f778ce1534f5 |
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| Source note | uspto-grants-1992_07 |
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