HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorobenzyl alcohol → 2-(2,4-Dichlorobenzyloxy)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorobenzyl alcohol | HCID 15684 | — |
| Reactant | 2-Methylthio-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine | HCID 59753914 | — |
| Product | 2-(2,4-Dichlorobenzyloxy)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine | HCID 59753957 | — |
Reaction Steps
2-Methylthio-5-(4-chlorophenyl)-4-(2,4-dichlorophenyl)pyrimidine from Reference Example 3 was reacted with 2,4-dichlorobenzyl alcohol according to the procedure described in Example 59 to afford 2-(2,4-dichlorobenzyloxy)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine (HRf): HPLC/MS: m/e=509 (M++1); Rt=5.07 min; 1H-NMR 400 MHz (CDCl3): δ 5.60 (s, 2H), 7.04 (d, J=9 Hz, 2H), 7.21 (m, 6H), 7.38-7.42 (m, 1H), 7.60 (d, J=9 Hz, 1H), 8.60 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405221B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-517dd2a1920c4388a6546b4daf4bd0c5 |
| Source note | uspto-grants-2008_07 |