HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20133554, compound → HCID 20184724, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20133554 | HCID 20133554 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20184724 | HCID 20184724 | 195.6% |
Reaction Steps
This compound was obtained by using the same procedure as that described in Example 8(b), by treating 9 g of 1,8-dihydroxy-10-cyclohexylcarbonylanthrone with 150 cm3 of acetic anhydride. After 3 hours the mixture was concentrated, and the oil obtained crystallized out by agitation in hexane. After the solvents had been sucked off, the 11 g of product obtained was dissolved in 150 cm3 of toluene heated to 100° C. and stirred in the presence of 10 g of silica gel. After a few minutes, the solution was filtered and the filtrate was cooled to 0° C. In this way 6 g of light-beige crystals of 1,8-diacetoxy-10-cyclohexylcarbonylanthrone having a melting point of 188° C. was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04696941 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-485b22f909e745bb83797470e304ab3b |
| Source note | uspto-grants-1987_09 |