HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007879Generated: October 30, 2026
1-Chloro-2-(diethylamine)ethane hydrochloride → HCID 10221262, compound
https://huagongshe.com/reaction/1007879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-2-(diethylamine)ethane hydrochloride | HCID 13363 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(1-Benzothiophen-5-yl)ethan-1-ol | HCID 11983371 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10221262 | HCID 10221262 | 99.6% |
Reaction Steps
In a mixture of 10 mL of 50% (W/V) aqueous solution of sodium hydroxide and 2 mL of toluene is suspended 2.00 g of 2-benzo[b]thiophen-5-yl-1-ethanol. To the suspension are added 2.51 g of N-(2-chloroethyl)-N,N-diethylamine hydrochloride and 0.38 g of tetra-n-butylammonium hydrogen sulfate, and the resulting mixture is heated under reflux for one hour. Water and toluene are added to the reaction mixture, and the organic layer is separated. The organic layer is washed successively with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, the solvent is distilled off under reduced pressure, and the residue is purified by column chromatography (eluent:chloroform:methanol=10:1) to obtain 3.10 g of N-[2-(2-benzo[b]thiophen-5-ylethoxy)ethyl]-N,N-diethylamine as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06797726B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-a9cec6b8a27f48128fe3cabf22881587 |
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| Source note | uspto-grants-2004_09 |
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