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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant(2-Cyclohexen-1-ylsulfonyl)benzeneHCID 4622731—
ReactantBenzyl 2-bromoethyletherHCID 57064374—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[2-(1-Benzenesulfonyl-cyclohex-2-enyl)-ethoxymethyl]-benzeneHCID 59152663—

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354431B2
Source datasetuspto-grants-2013_01
ORD IDord-fdbba50777574fc99442d37cf3c29c3a
Source noteuspto-grants-2013_01