HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249210Generated: November 1, 2026
Carbon Disulfide → HCID 178455738, compound
https://huagongshe.com/reaction/249210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 178455737 | HCID 178455737 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178455738 | HCID 178455738 | 72.7% |
Reaction Steps
A mixture of 1-phenyl-2-(trans-4-ethylcyclohexyl)ethane (200.0 g, 0.93 mol), pulverized succinic acid anhydride (111.6 g, 1.11 mol) and CS2 (500 ml) was cooled with ice down to 0° to 5° C. Pulverized anhydrous aluminum chloride (248.0 g, 1.86 mol) was gradually added to the mixture. After removing the ice bath, the mixture was agitated for one hour and successively agitated for 2 hours on a water bath at 60° C. The resulting material was allowed to stand overnight. The reaction material was poured into a mixture of ice (500 g) and 6N-HCl (300 ml). The mixture was agitated sufficiently and CS2 and water were distilled off on a water bath, to obtain a residue. Toluene was added to the residue and then heated under reflux. After separating water by means of a DeanStoke type water separator, the resulting liquid was filtered off while hot and recrystallized to obtain the following 3-(4-(2-(trans-4-ethylcyclohexyl)ethyl)benzoyl)propanic acid (214 g, m.p.: 141.2°-142.6° C.). ##STR8##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05213708 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-f9babbfe4002489da777b4b233cf2a06 |
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| Source note | uspto-grants-1993_05 |
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