HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359696Generated: October 29, 2026
1,2-Dichloroethane → HCID 14580245, compound
https://huagongshe.com/reaction/359696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dihydro-3(2H)-thiophenone | HCID 61252 | — |
| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 14580245 | HCID 14580245 | 14.5% |
Reaction Steps
Anthranilonitrile (4.80 g) and tetrahydrothiophen-3-one (8.17 g) were stirred until a homogeneous mixture was obtained and then fresly fused ZnCl2 (8.0 g) was added and the reaction mixture heated at 120°. After 2 hours, 30 ml of 1,2-dichloroethane was added and the reaction mixture refluxed for an additional 2 hours. At the end of this time the reaction mixture was distributed between 10% NaOH solution and 2-butanone, after which the organic phase was separated, dried, concentrated and purified by flash chromatography (5% i-PrOH/CH2Cl2). Combination of the product-containing fractions gave 1.19 g of product that was pure to thin layer chromatography. This product was combined with that obtained in another run and recrystallized from EtOAc-pentane to give analytically pure material, mp 220° (d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05002955 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-b7ba5dc92fab4b398b94a6f6054b8c4e |
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| Source note | uspto-grants-1991_03 |
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