Water → HCID 53853952、化合物
反応式
[CH2:1]([O:4][CH2:5][C:6]1[C:7]([Cl:25])=[N+:8]([O-:24])[C:9]([CH2:20][CH:21]([CH3:23])[CH3:22])=[C:10]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:11]=1)[CH:2]=[CH2:3].C(N(C(C)C)CC)(C)C.O>C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Cl-].[Rh].C(O)C>[CH:1]([O:4][CH2:5][C:6]1[C:7]([Cl:25])=[N+:8]([O-:24])[C:9]([CH2:20][CH:21]([CH3:22])[CH3:23])=[C:10]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:11]=1)=[CH:2][CH3:3]参加物
6
実験手順
To 200 mg of 3-allyloxymethyl-5-benzyloxy-2-chloro-6-isobutylpyrazine 1-oxide were added 195 μl of diisopropylethylamine, 51 mg of a Wilkinson's catalyst ##STR69## and 4 ml of water (10% volume)-ethanol. The mixture was reacted for 3 hours at 85°-90° C. The catalyst was removed by filtration to obtain 260 mg of 3-(1-propenyl)oxymethyl-5-benzyloxy-2-chloro-6-isobutylpyrazine 1-oxide (Compound B-6) [a cis/trans (about 4/3) mixture] as a colorless oily substance.
後処理
- customThe mixture was reacted for 3 hours at 85°-90° C
- customThe catalyst was removed by filtration
出典と根拠
- ORDレコード
- ord-a38aed4ca8f64a11bc212e68fca3eb39
- 出典データセット
- uspto-grants-1993_08
- 特許番号
- US05238938
反応ノート
読み込み中…