HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chrysenecarbaldehyde → 12-Ethoxychrysene-6-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chrysenecarbaldehyde | HCID 12438774 | — |
| Reactant | 6-Ethoxychrysene | HCID 14423315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 12-Ethoxychrysene-6-carbaldehyde | HCID 13375391 | 64% |
Reaction Steps
6-Ethoxychrysene (Cambridge Chemical, Inc., 48 g, 0.176 mol) was formylated according to the procedure outlined in 1A, except that CH2Cl2 (1 L) was used as the reaction solvent. After isolation, the crude material was chromatographed on a plug of SiO2 (500 g) using CH2Cl2 as the eluting solvent to give (after removal of solvent and drying) 33.7 g (64%) of 12-ethoxychrysene-6-carbaldehyde mp 173.5°-176°, (C, H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810727 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-e6096158fd93495dbc6dc5a93b1ef732 |
| Source note | uspto-grants-1989_03 |