HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroanthraquinone → Anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroanthraquinone | HCID 8553 | — |
| Reactant | 1-Methoxyethanol | HCID 3015637 | — |
| Solvent | Methylenechloride Hexane | HCID 21226440 | — |
| Product | Anthraquinone | HCID 6780 | — |
Reaction Steps
Using the procedure outlined in Examples 1A, 2-chloroanthraquinone (Aldrich) and methoxyethanol (Aldrich) gave a 44.3% yield of 2-[2-(methoxy)ethoxy)]anthraquinone, mp 126°, (C,H), (CH2Cl2 /hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05241107 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-ea45f38d2a8b47f088d75505c8addc9a |
| Source note | uspto-grants-1993_08 |