HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274344Generated: October 25, 2026
Ammonium Chloride → HCID 20093195, compound
https://huagongshe.com/reaction/274344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,4-Oxathiane | HCID 27596 | — |
| Reactant | 4-Bromo-1,2-dichlorobenzene | HCID 29013 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Chloro-1,4-oxathiane | HCID 15248366 | — |
| Reactant | HCID 178478192 | HCID 178478192 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20093195 | HCID 20093195 | — |
Reaction Steps
A stirred solution of 3,4-dichlorophenylmagnesium bromide [prepared from 3,4-dichlorobromobenzene (10.2 g, 45 mmol) and magnesium (1.1 g, 45 mmol) in the usual fashion] was treated with a solution of 3-chloro-1,4-oxathiane [prepared from 1,4-oxathiane (2.6 g, 25 mmol) using the method of Tuleen and Bennet J. Het. Chem. 1969, 6, 115] in benzene (30 ml), maintaining the temperature of reaction below 10° C. The mixture was allowed to stand at room temperature overnight. It was then poured into ammonium chloride solution (50 ml), the organic phase was separated and the aqueous washed with ether (2×40 ml). The combined organic extracts were dried (MgSO4) and purified by flash chromatography on silica eluting with toluene/hexane (1:1) to give 3-(3,4-dichlorophenyl)-1,4-oxathiane (4.5 g), as colourless crystals, m.p. 65°-68° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389649 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-d3d59d9db8ea4c979eed8b03df0a62de |
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| Source note | uspto-grants-1995_02 |
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