反応式
[Li].ClC1C=CC=CC=1C.Br[C:11]1[CH:16]=[CH:15][C:14]([C:17]2[O:18][CH:19]=[N:20][N:21]=2)=[CH:13][CH:12]=1.C([Li])CCCCC.C[O:30][B:31](OC)[O:32]C>C1COCC1.C1(C2C=CC=CC=2)C=CC=CC=1.CC(C)CC(=O)C.CO>[O:18]1[CH:19]=[N:20][N:21]=[C:17]1[C:14]1[CH:15]=[CH:16][C:11]([B:31]([OH:32])[OH:30])=[CH:12][CH:13]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- -30 °C
実験手順
Tetrahydrofuran (250 g) was charged to a mixture of lithium granules (3.02 g) and biphenyl (0.01 g) under an argon atmosphere and the mixture cooled to −30° C. 2-Chlorotoluene (27.55 g) was slowly added at −30° C. The reaction was held at −30° C. for 6 hours and then cooled to −65° C. A mixture of 2-(4-bromophenyl)-1,3,4-oxadiazole (50.0 g) in THF (300 g) was slowly added at −65° C. The reaction was held at −65° C. for 30 minutes then a solution of n-hexyllithium (33% w/w in hexanes, 86 ml) was added at −65° C. The reaction was held at −65° C. for 30 minutes and then trimethylborate (48.7 g) was added at −65° C. The reaction was held at −65° C. for 10 minutes then methanol (55.3 g) was added followed by 4-methyl-2-pentanone (240 g). The reaction mixture was warmed and the low boiling solvents distilled off under vacuum to a maximum temperature of 55° C. The residual mixture was cooled to 0° C. and 10% w/w sulphuric acid (92 g) was added followed by water (92 g) whilst maintaining the temperature below 7° C. Product precipitated. The pH was adjusted to 6.5 by the addition of more 10% w/w sulphuric acid (85.3 g). The mixture was heated to 40° C. then cooled back to 5-10° C. Product was isolated and washed with THF (56 g) and water (60 g), yielding wet title compound (25.2 g, 60%).
後処理
- temperaturecooled to −65° C
- additionwas slowly added at −65° C
- waitThe reaction was held at −65° C. for 30 minutes
- waitThe reaction was held at −65° C. for 30 minutes
- waitThe reaction was held at −65° C. for 10 minutes
- temperatureThe reaction mixture was warmed
- distillationthe low boiling solvents distilled off under vacuum to a maximum temperature of 55° C
- temperatureThe residual mixture was cooled to 0° C.
- addition10% w/w sulphuric acid (92 g) was added
- temperaturewhilst maintaining the temperature below 7° C
- customProduct precipitated
- additionThe pH was adjusted to 6.5 by the addition of more 10% w/w sulphuric acid (85.3 g)
- temperatureThe mixture was heated to 40° C.
- temperaturethen cooled back to 5-10° C
- customProduct was isolated
- washwashed with THF (56 g) and water (60 g)
出典と根拠
- ORDレコード
- ord-72daac1cb498489f821f0afb99bf6bee
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07626020B2
関連ノート
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