HuagongsheHuagongshe Chemistry Print Report · For research reference only
Heptylbenzene → HCID 54486030, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Heptylbenzene | HCID 14115 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | (-)-trans-1,2-Cyclohexanedicarboxylic Anhydride | HCID 12261141 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 54486030 | HCID 54486030 | — |
Reaction Steps
Trans-1,2-cyclohexanedicarboxylic anhydride (6.76 g , 0.044 mole) was heated with 1-phenylheptane (100 ml) and anhydrous aluminum chloride (12.86 g, 0.096 moles) at 100° C. for 1 hour. The reaction mixture was then poured into a mixture of ice water (500 ml) and concentrated hydrochloric acid (50 ml). The product was extracted with ether (2×200 ml) and the extracts dried over magnesium sulfate and filtered. The ether was removed under reduced pressure and the remaining solution chromatographed on silica (hexane and then hexane:ether:acetic acid at 70:30:1) to yield trans-2-(4-heptylbenzoyl) cyclohexane-1-carboxylic acid (7.36 g), m.p. 91°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05504244 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-ad93d9dc0d734e5586042c28a254a0f3 |
| Source note | uspto-grants-1996_04 |