HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839162Generated: October 30, 2026
Carbon Dioxide → 7-(4-Methoxyphenyl)heptyl phenyl sulfide
https://huagongshe.com/reaction/839162
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Thioanisole | HCID 7520 | — |
| Reactant | HCID 14977896 | HCID 14977896 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(4-Methoxyphenyl)heptyl phenyl sulfide | HCID 20389987 | — |
Reaction Steps
Phenyllithium (378 ml., 0.755 mole) was added over a period of 2-5 minutes to a solution of 94.5 g. of thioanisole in 600 ml. of tetrahydrofuran, stirred under nitrogen. The mixture was stirred at room temperature for about 16 hours, then cooled to -70° C. (solid CO2), and 141 g. of 6-(4-methoxyphenyl)hexyl iodide in 210 ml. of tetrahydrofuran was added slowly. The reaction mixture was stirred at -65° C. for 2 hours and then allowed to warm to room temperature. Water was added and the mixture extracted with pentane. The pentane extracts were washed with water, dried and concentrated to remove the solvent. The residue was distilled in vacuo, b.p. 171°-174° C. (0.15 mm.). The distillate crystallized and was recrystallized from pentane, to give 7-(4-methoxyphenyl)heptyl phenyl sulfide, m.p. 58°-59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093736 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-a638036b5dba45769a6e9b7d5f0c2bf3 |
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| Source note | uspto-grants-1978_06 |
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