反応式
[CH3:1][O:2][C@@H:3]1[O:18][C@H:17]([CH2:19][O:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[Cl:29])[C@@H:6]([O:7][CH2:8][C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=2[Cl:16])[C@@:4]1(C)[OH:5]>C(Cl)Cl>[CH3:1][O:2][C@@H:3]1[O:18][C@H:17]([CH2:19][O:20][CH2:21][C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][C:23]=2[Cl:29])[C@@H:6]([O:7][CH2:8][C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=2[Cl:16])[C@H:4]1[OH:5]参加物
反応条件
- 温度
- 3 °C
実験手順
To a solution of the product of Step 1 (171.60 g, 0.2676 mol) in 1.8 L of methylene chloride that was cooled to 0° C., was added dropwise a solution of stannous chloride (31.522 mL, 0.2676 mol) in 134 mL of methylene chloride while stirring. After maintaining the solution at about 3° C. for approximately 27 hours, another 5.031 mL of stannous chloride (SnCl4) (0.04282 mol) was added and the solution was kept at about 3° C. overnight. After a total reaction time of approximately 43 hours, the reaction was quenched by carefully adding the solution to 1.9 L of a saturated NaHCO3 solution. Tin salts were removed via filtration through Celite after which the organic phase was isolated, dried with MgSO4 and evaporated in vacuo. The yield of raw, dark yellow oil was 173.6 g. The crude oil was used directly in the next step without further purification.
後処理
- customAfter a total reaction time of approximately 43 hours, the reaction was quenched
- additionby carefully adding the solution to 1.9 L of a saturated NaHCO3 solution
- customTin salts were removed via filtration through Celite after which the organic phase
- customwas isolated
- dry with materialdried with MgSO4
- customevaporated in vacuo
- customThe crude oil was used directly in the next step without further purification
出典と根拠
- ORDレコード
- ord-49e01139168c44119d68b0be19688782
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07244713B2
関連ノート
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