HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Allyl-3-methylcyclobutanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Methylcyclobutan-1-one | HCID 15199 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Product | 1-Allyl-3-methylcyclobutanol | HCID 67305235 | 46.9% |
Reaction Steps
Methylcyclobutanone (3.200 g, 38.043 mmol) was dissolved in 200 ml THF and allylmagnesium bromide (190.21 ml, 190.21 mmol) was added in one portion. The mixture was stirred for 4 h at RT, hydrolyzed with water and extracted. The combined organic extracts were dried over MgSO4 and evaporated and purified via glass col. Chrom. (25-75% hex. in EtOAc). 1-Allyl-3-methylcyclobutanol (2.250 g, 46.9% yield) was obtained as a mixture of cis-trans isomers approx 4:1 (where the major compound is the one Me-cis to OH) based on NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745484B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-5a21bab2a39b4e56a4ba1ff98b5872cb |
| Source note | uspto-grants-2010_06 |