HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5227Generated: October 26, 2026
Thionyl Chloride → O-methyl (4'-methylbiphenyl-2-yl)carbonylthiocarbamate
https://huagongshe.com/reaction/5227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(4-Methylphenyl)benzoic acid | HCID 81568 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | O-methyl (4'-methylbiphenyl-2-yl)carbonylthiocarbamate | HCID 54295303 | — |
Reaction Steps
In chloroform (40 ml) was dissolved (4'-methylbiphenyl-2-yl)carboxylic acid (10 g). To the solution was added thionyl chloride (7 ml), and the mixture was heated for 3 hours under reflux. The reaction mixture was poured into ice-water, then the organic layer was separated, washed with water and concentrated to dryness to give a syrup, which was dissolved in dioxane (80 ml). To the solution was added powdered potassium thiocyanate (9.16 g), and the mixture was heated for one hour under reflux. The reaction mixture was allowed to cool, and then insolubles were filtered off. After addition of methanol (15 ml) to the filtrate, the solution was heated for 15 minutes under reflux. The reaction solution was concentrated to dryness, and the resulting crystals were crystallized from isopropyl ether to afford the title compound as white plates (7.4 g, 55%),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05243054 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-3530d84ddd434b9796c4ba61b9c55ed4 |
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| Source note | uspto-grants-1993_09 |
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