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alpha,4-Dichloroanisole → 2-(4-Chlorophenoxymethyl)thio-5-chloropyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | alpha,4-Dichloroanisole | HCID 88801 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | 5-Chloro-2(1H)-pyrimidinethione | HCID 7140345 | — |
| 溶媒 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 生成物 | 2-(4-Chlorophenoxymethyl)thio-5-chloropyrimidine | HCID 20475741 | 70% |
反応手順
A mixture of p-chlorophenoxymethyl chloride (6 mmol) and the potassium salt of 5-chloropyrimidine-2-thione (5 mmol) in 1,2-dimethoxyethane (25 ml) was stirred at room temperature for 10 h, the solvent distilled off at reduced pressure, the residue extracted with chloroform (70 ml), the chloroform (70 ml), the chloroform solution washed with 1 M NaOH (2×10 ml) and water (10 ml), and the dried (MgSO4) solution evaporated. The residual sulfide was recrystallized from iPrOH; yield 70%, m.p. 120° C. 1H NMR (DMSO-d6): δ5.90 (SCH2), 6.98 and 7.31 (Ph), 8.78 (H-4, H-6).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04423047 |
| 出典データセット | uspto-grants-1983_12 |
| ORD ID | ord-6850c6687dd74eae85231a8410eefbdd |
| 出典メモ | uspto-grants-1983_12 |