HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968986Generated: October 25, 2026
Water → Benzyl 1-methyl-4-oxocyclohexane-1-carboxylate
https://huagongshe.com/reaction/1968986
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl methacrylate | HCID 17236 | — |
| Reactant | 1-(Trimethylsiloxy)-1,3-butadiene | HCID 2724217 | — |
| Catalyst | 4,4'-Methylenebis(2,6-di-tert-butylphenol) | HCID 8372 | — |
| Product | Benzyl 1-methyl-4-oxocyclohexane-1-carboxylate | HCID 59444129 | 24.89% |
Reaction Steps
2-(Trimethylsilyloxybutadiene (6.46 g, 45.4 mmol), phenylmethyl 2-methyl-2-propenoate (8.00 g, 45.4 mmol), and 4,4′-methanediylbis[2,6-bis(1,1-dimethylethyl)phenol] (0.019 g, 0.045 mmol) were combined together in a 20.0 mL microwave vessel and heated to 200° C. for 300 mins. Sample recovered and removed from vessel using THF (˜3×10 mL). The solvent was removed under reduced pressure and the residual oil taken up in 10% 2N HCl/THF (100 mL) and stirred overnight. After this time a clear solution formed, which was diluted with water (50 mL), partitioned into DCM (2×100 mL) and the organic layers separated, dried over MgSO4, filtered and the solvent removed under reduced pressure. The residue was purified by FC over Silica (150 g: 5-10% EtOAc/iso-hex) to afford a clear oil. Confirmed by NMR to be phenylmethyl 1-methyl-4-oxocyclohexanecarboxylate (3.48 g, 11.30 mmol, 24.89% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426443B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-ec0c866b03c24aa4863501511263fac8 |
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| Source note | uspto-grants-2013_04 |
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