HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → 1,5-Dioxaspiro[5.5]undec-3-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Trimethylolmethane | HCID 78432 | — |
| Product | 1,5-Dioxaspiro[5.5]undec-3-ylmethanol | HCID 15286693 | 65% |
Reaction Steps
The same procedure as in the step (1a) of Example 1 was repeated using 2-(hydroxymethyl)-1,3-propanediol and cyclohexanone to obtain the title compound (2.26 g, yield: 65%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425634B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-5cb5e6131adb45fb800cd2a1b6dcb053 |
| Source note | uspto-grants-2008_09 |