HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632555Generated: October 29, 2026
Toluene → 4-Methylcyclohex-3-ene-1-carbonyl chloride
https://huagongshe.com/reaction/632555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (1S)-4-methylcyclohex-3-ene-1-carboxylic acid | HCID 10877190 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methylcyclohex-3-ene-1-carbonyl chloride | HCID 12951475 | — |
Reaction Steps
(1S)-4-Methyl-cyclohex-3-enecarboxylic acid (209 mg, 1.5 mmol), azeotropically dried by evaporation from toluene, was treated with potassium phosphate tribasic (383 mg, 1.8 mmol), suspended in dichloromethane (4 mL) and treated with dimethylformamide (2 drops). The reaction mixture was cooled to 0° C. and treated dropwise with oxalyl chloride (0.3 mL, 3.2 mmol). The reaction mixture was allowed to warm to ambient temperature while stirring for 2 h. After filtering the solids, the solution was concentrated, treated with hexanes and concentrated again to afford 4-methyl-cyclohex-3-enecarbonyl chloride (S) as a light yellow oil which was used immediately in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321753B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-da5a45d537f74724b9571127e03430d5 |
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| Source note | uspto-grants-2016_04 |
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