HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dichlorobenzyl alcohol → 2-(3,4-Dichlorobenzyloxy)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dichlorobenzyl alcohol | HCID 15728 | — |
| Reactant | 2-Methylthio-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine | HCID 69198971 | — |
| Product | 2-(3,4-Dichlorobenzyloxy)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine | HCID 59753926 | — |
Reaction Steps
2-Methylthio-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine from Reference Example 3 was reacted with 3,4-dichlorobenzyl alcohol according to the procedure described in Example 59 to afford 2-(3,4-dichlorobenzyloxy)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine (HRf): HPLC/MS: m/e=509 (M++1); Rt=5.14 min; 1H-NMR 400 MHz (CDCl3): δ 5.56 (s, 2H), 7.12 (d, J=9 Hz, 1H), 7.22-7.25 (m, 4H), 7.27-7.40 (m, 3H), 7.28 (m, 1H), 7.68 (d, J=2 Hz, 1H), 8.45 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405221B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-4add91d495224f189934618517225d66 |
| Source note | uspto-grants-2008_07 |