HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354524Generated: October 29, 2026
Acetyl chloride → 2-Methyl[1,1'-bi(cyclohexane)]-2-yl acetate
https://huagongshe.com/reaction/354524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20507686 | HCID 20507686 | — |
| Solvent | N,N-Dimethylaniline | HCID 949 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methyl[1,1'-bi(cyclohexane)]-2-yl acetate | HCID 20507685 | — |
Reaction Steps
A mixture of 360 ml of acetyl chloride and 153 ml of acetic acid anhydride is added dropwise at 0° C., whilst stirring, to a solution of 576 g of crude 1-methyl-2-cyclohexyl-cyclohexanol in 750 ml of N,N-dimethylaniline. The mixture is then allowed to come to room temperature, after which is heated to 40° C. for 36 hours. Thereafter, the reaction mixture is poured onto ice and diluted with 1 liter of ether, and the organic phase is separated off and concentrated on a Rotavapor apparatus. The residue is then taken up in 2 liters of ether and the solution is washed with three times 200 ml of cold 2-N HCl and then with saturated bicarbonate solution and water until neutral, and is dried with anhydrous MgSO4 and evaporated in vacuo. 646 g of crude 1-acetoxy-1-methyl-2-cyclohexyl-cyclohexane are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04375428 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-17873164b51c4ef2804cf4fa49058b25 |
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| Source note | uspto-grants-1983_03 |
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