HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078757Generated: October 27, 2026
1,5-Dibromopentane → 4-[6-Bromo-1-[(4-methylphenyl)thio]hexyl]-1,2-dimethoxybenzene
https://huagongshe.com/reaction/1078757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | 1,2-Dimethoxy-4-[[(4-methylphenyl)thio]methyl]benzene | HCID 10516471 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[6-Bromo-1-[(4-methylphenyl)thio]hexyl]-1,2-dimethoxybenzene | HCID 10812203 | — |
Reaction Steps
A solution of 13.72 g of 1,2-dimethoxy-4-[[(4-methylphenyl)thio]methyl]benzene in 200 mL of tetrahydrofuran (dried over 3A sieves), under nitrogen, is cooled to -78° C. and 30 mL of 1.7M t-butyl lithium is added. After 30 minutes, the solution is transferred, via a canula, into a stirred solution of 14.0 mL of 1,5-dibromopentane in 25 ml of tetrahydrofuran, under nitrogen at -78° C. The reaction is slowly warmed to room temperature, and the reaction is quenched by the addition of 4 mL of acetone. The reaction is concentrated in vacuo and the residual material is dissolved in ethyl acetate and is washed with brine. Drying (sodium sulfate) and solvent removal affords 33.22 g of oil. The residue is purified via chromatography on silica gel with gradient elution progressing from hexane to chloroform to methyl alcohol to afford 10.82 g of the desired product as a tan gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05550149 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-ec068432e1c14ef9a94425329533183e |
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| Source note | uspto-grants-1996_08 |
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