HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681331Generated: November 4, 2026
Ethane, 1-chloro-2-ethoxy- → HCID 19806348, compound
https://huagongshe.com/reaction/1681331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethane, 1-chloro-2-ethoxy- | HCID 12341 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178526030 | HCID 178526030 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19806348 | HCID 19806348 | 9,281.9% |
Reaction Steps
Dissolved in 2.5 ml of N,N-dimethylformamide were 0.50 g of 2-mercapto-4-(3-pyridyl)-thiazole oxalate (1.82 mmol), and 0.10 g (4.17 mmol) of sodium hydride were added to the solution, which was stirred at room temperature. One hour later, 0.40 ml (3.65 mmol) of 2-chloroethyl ethyl ether were added to the suspension, which was then stirred for 2 hours at 80° C. The reaction solution was diluted with 50 ml of chloroform, followed by addition of 50 ml of a 5% saline solution and washing. After separation of the chloroform layer, the organic layer was dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residues were then purified by silica gel chromatography to obtain 45 g of the title compound as an yellow oily form (93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05171746 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-927fbf6520ad4aeb880e79b30bb805ac |
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| Source note | uspto-grants-1992_12 |
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