HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804763Generated: October 30, 2026
Hexane → [2-(1-Benzenesulfonyl-cyclohex-2-enyl)-ethoxymethyl]-benzene
https://huagongshe.com/reaction/1804763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | (2-Cyclohexen-1-ylsulfonyl)benzene | HCID 4622731 | — |
| Reactant | Benzyl 2-bromoethylether | HCID 57064374 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(1-Benzenesulfonyl-cyclohex-2-enyl)-ethoxymethyl]-benzene | HCID 59152663 | — |
Reaction Steps
Cyclohex-2-enesulfonyl-benzene (7) (10 g, 45 mmol) is dissolved in 450 ml of dry THF and cooled down to −20° C. Then 1.6 M BuLi in Hexane (30.9 ml, 49.5 mmol) is added and stirred for 15 min. After addition of benzyl 2-bromoethylether (8.5 ml, 54 mmol) the mixture is stirred for 1 h at 0° C. Then the mixture is evaporated to dryness. The residue is treated with ice/1M HCl and extracted twice with ether. The combined organic layers are dried over Na2SO4 and evaporated under educed pressure. The product is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354431B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-fdbba50777574fc99442d37cf3c29c3a |
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| Source note | uspto-grants-2013_01 |
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