HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522538Generated: November 2, 2026
Benzenesulfonyl chloride → 5-Bromo-2-butylbenzofuran
https://huagongshe.com/reaction/522538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Bromo-2-formylphenoxy)hexanoic acid | HCID 22057826 | — |
| Reactant | Ethyl acetate methylcyclohexane | HCID 66985183 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromo-2-butylbenzofuran | HCID 56926023 | — |
Reaction Steps
25.8 ml of benzenesulfonyl chloride (0.202 mol; 1.4 equivalents) and 40 ml of toluene are placed in an equipped reactor and the mixture is stirred at 80° C. 65 ml of anhydrous triethylamine (0.47 mol) and then 45.2 g of 2-(4-bromo-2-formylphenoxy)hexanoic acid (compound VIII) (0.144 mol) dissolved in 250 ml of toluene are then added slowly at 80° C. The reaction progress is monitored by TLC (eluent: 80/20 methylcyclohexane/ethyl acetate; Rf of compound VIII=0.08; Rf of the desired compound IX=0.80).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334254B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-aaf4388929724f84b3113c0b1d7d133a |
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| Source note | uspto-grants-2016_05 |
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