HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494261Generated: October 30, 2026
1,6-Dibromohexane → 1-(6-Bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene
https://huagongshe.com/reaction/1494261
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | HCID 12950402 | HCID 12950402 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(6-Bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene | HCID 14986441 | 15% |
Reaction Steps
To 27.0 g (0.139 mole) of 1,2-dimethoxy-3-(1,1-dimethylethyl)benzene in 350 mL of anhydrous tetrahydrofuran cooled in an ice-brine bath at -5° was added. 87 mL (0.139 mole) of 1.6M butyl lithium in hexane over 30 minutes. The reaction mixture was stirred at -5° for 3 hours and then at reflux for 1 hour. After cooling in an ice bath, 21.5 mL (0.139 mole) of 1,6-dibromohexane in 75 mL of tetrahydrofuran was added dropwise. The reaction mixture was then stirred at reflux for 17 hours. The solvent was removed under reduced pressure, 50 mL of 3N hydrochloric acid was added and the product was extracted with ether. The extract was washed with sodium bicarbonate solution, dried and concentrated at reduced pressure to an oil. Purification by HPLC using 20% toluene-hexane gave 7.6 g ((15% yield) of 1-(6-bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05025036 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-c374b92fbf8045c0b99ec29fd43025a0 |
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| Source note | uspto-grants-1991_06 |
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