HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 44511908, compound → (2S,3R,4S)-2,3,4-Trihydroxycyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 44511908 | HCID 44511908 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | (2S,3R,4S)-2,3,4-Trihydroxycyclohexanone | HCID 45082801 | — |
Reaction Steps
The method for producing catechol as described above, by dehydrating 2-deoxy-scyllo-inosose while heating to give (4S,5R,6S)-4,5,6-trihydroxy-2-cyclohexene-1-one, and then reducing the (4S,5R,6S)-4,5,6-trihydroxy-2-cyclohexene-1-one with hydrogen in the presence of a metal catalyst to give (2S,3R,4S)-2,3,4-trihydroxycyclohexane-1-one, and then further dehydrating the (2S,3R,4S)-2,3,4-trihydroxycyclohexane-1-one while heating.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08378146B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-bc0de22eb71242749ef01d71d98ef844 |
| Source note | uspto-grants-2013_02 |