HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053488Generated: November 3, 2026
Toluene → (R)-4-methylcyclohex-3-enecarbonyl chloride
https://huagongshe.com/reaction/1053488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (R)-4-methylcyclohex-3-enecarboxylic acid | HCID 11040781 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-4-methylcyclohex-3-enecarbonyl chloride | HCID 58113947 | — |
Reaction Steps
(R)-4-methylcyclohex-3-enecarboxylic acid 503 (371 mg, 2.65 mmol), azeotropically dried by evaporation from toluene, was treated with potassium phosphate tribasic (1.13 g, 7.94 mmol), suspended in dichloromethane (7.6 mL) and treated with dimethylformamide (4 drops). The reaction mixture was cooled to 0° C. and treated dropwise with oxalyl chloride (0.75 mL, 7.9 mmol). The reaction mixture was allowed to warm to ambient temperature while stirring for 2 hours. After filtering the solids, the solution was concentrated, treated with hexanes and concentrated again to afford (R)-4-methylcyclohex-3-enecarbonyl chloride 504 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 | US09393256B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ac7c92ad7b6e41b597e8c17143a86c37 |
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| Source note | uspto-grants-2016_07 |
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