HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749231Generated: October 30, 2026
1,6-Dibromohexane → 6-Bromohexylbut-3-ynyl ether
https://huagongshe.com/reaction/749231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | 3-Butyn-1-OL | HCID 13566 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 6-Bromohexylbut-3-ynyl ether | HCID 11379281 | 31.1% |
Reaction Steps
A mixture of 50% w/v aqueous sodium hydroxide (2500 ml), 1,6-dibromohexane (2610 g) and tetra-butylammonium bromide (25 g) was warmed to 50° C., with stirring. But-3-yn-1-ol (500 g) was then added to the reaction mixture at such a rate as to ensure the content's temperature did not exceed 65° C. The reaction was left at 50° C. overnight before being cooled to room temperature. Tert-butyl methyl ether (2500 ml) and brine (2000 ml) was added to the cooled mixture and the layers allowed to separate. The ethereal layer was washed with water (2×2000 ml), brine (1×2000 ml), and then dried over anhydrous MgSO4. The solution was filtered and concentrated under reduced pressure to give crude product as a liquid. This was further purified by fractional distillation using a 60 cm vacuum jacketed Vigreux column at ca. 0.5 mbar. The product was obtained in the fraction which boiled at 92-98° C., to give the title compound (518 g), LC RT=6.16 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402598B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-c9086713e4184255946362b034db2296 |
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| Source note | uspto-grants-2008_07 |
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