Trifluoroacetic acid → HCID 68502963、化合物
反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1/[CH:8]=[CH:9]/[C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=1[O:17]C(=O)C.F[C:22](F)(F)[C:23](O)=O.CO[CH2:30][N:31]([Si](C)(C)C)C>C1(C)C=CC=CC=1>[CH3:30][N:31]1[CH2:23][CH2:22][C@@H:9]([C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=2[OH:17])[C@@H:8]1[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[Br:1]参加物
実験手順
trans-2-Bromo-2′-acetoxy-5′-chlorostilbene (26 g, 73 mmol) was slurried in toluene (91 ml) at 33° C. Trifluoroacetic acid (200 microliters) was added. The N-methoxymethyl-N-trimethylsilyl-N-methylamine (14.5 g; 89.7 mmol) was added to the reaction mixture over 90 minutes. After addition, the reaction was washed with water (25 ml). The toluene was removed by vacuum distillation. Ethanol (30 ml) was added and removed under reduced pressure. The oil was dissolved in methanol (90 ml). Potassium hydroxide (5 grams in 25 ml water)) was added. The product began to precipitate immediately. After 30 minutes, the pH was adjusted to 8-9 with 3N HCl (8 ml). Added water (10 ml) and cooled to less than 10° C. Filtered and washed with 1:1 methanol: water. Dried in vacuum to 26.0 grams (96% yield). Purity according to HPLC is 98% a/a.
後処理
- additionAfter addition
- washthe reaction was washed with water (25 ml)
- customThe toluene was removed by vacuum distillation
- additionEthanol (30 ml) was added
- customremoved under reduced pressure
- dissolutionThe oil was dissolved in methanol (90 ml)
- additionPotassium hydroxide (5 grams in 25 ml water)) was added
- customto precipitate immediately
- temperatureAdded water (10 ml) and cooled to less than 10° C
- filtrationFiltered
- washwashed with 1:1 methanol
- customDried in vacuum to 26.0 grams (96% yield)
出典と根拠
- ORDレコード
- ord-2b01e92ede874a0d857169e93da74062
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07750167B2
反応ノート
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