HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-((Benzyloxy)methyl)spiro[2.5]octane → Spiro[2.5]octan-4-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-((Benzyloxy)methyl)spiro[2.5]octane | HCID 67983984 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | Spiro[2.5]octan-4-ylmethanol | HCID 68083958 | — |
Reaction Steps
To a solution of 4-((benzyloxy)methyl)spiro[2,5]-octane (0.42 g, 1.8 mmol) in a 5:1 MeOH-EtOAc (12 mL) Pd/C (0.05 g, 5 wt %, 50% wet Degussa type) was added. The flask was fitted with a balloon of hydrogen, and the heterogeneous reaction mixture was stirred for 2 hours under a hydrogen atmosphere at rt. The catalyst solids were filtered off and the filtrate was concentrated under vacuum to give the desired product spyri[2.5]octan-4-ylmethanol as clear oil. 1H NMR (400 MHz, CDCl3) δ 3.74-3.62 (m, 2H), 3.48 (d, J=5.2 Hz, 2H), 1.65-1.59 (m, 2H), 1.51-1.43 (m, 3H), 1.27-1.24 (m, 1H), 1.12-1.11 (m, 1H), 0.96-0.95 (m, 1H), 0.41-0.37 (m, 1H), 0.29-0.17 (m, 3H). MS m/z 123.1 (M−17+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150568B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-4e2d1d55598a48dd94eb745ec25fbde8 |
| Source note | uspto-grants-2015_10 |