HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096176Generated: November 1, 2026
Methanol → Tert-Butyl 1-(2-oxoethyl)cyclopropanecarboxylate
https://huagongshe.com/reaction/1096176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Cyclopropanecarboxylic acid, 1-(2-propenyl)-, 1,1-dimethylethyl ester | HCID 546367 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-Butyl 1-(2-oxoethyl)cyclopropanecarboxylate | HCID 58817571 | 56% |
Reaction Steps
6.9 g (36.34 mmol, 1 eq., 96% a % by GC) 1-allyl-cyclopropanecarboxylic acid tert-butyl ester were dissolved in 40 ml CH2Cl2 and 40 ml MeOH. The solution was cooled to −72° C. and the ozone was bubbled through the reaction mixture until a blue color was obtained. Then nitrogen was bubbled to remove excess ozone until a colorless solution was obtained. 10 ml (3.68 eq.) dimethyl sulfide and 14 ml (2.76 eq.) triethylamine were added. The reaction mixture was warmed to RT and stirred overnight at that temperature (peroxide test negative, pH 7-8). The yellowish reaction mixture was added to 100 ml sat. aq. ammonium chloride solution (exothermic) and extracted 3 times with 70 ml CH2Cl2. The organic phases were combined, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide the crude aldehyde, which was purified by filtration over SiO2 (CH2Cl2; TLC:EtOAc/heptane 1:2) to provide 3.90 g (96% GC, 56% yield) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138175B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-44df0d0b3d6c46e8807a302005dade20 |
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| Source note | uspto-grants-2012_03 |
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