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Carbon Disulfide → Benzyl (4-phenyl)dithiobenzoate

HRID 1926558
ノート
印刷プレビュー

反応式

HRID 1926558 の反応式
[C:1]1([C:7]2[CH:12]=[CH:11][C:10]([Mg]Br)=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:15](=[S:17])=[S:16].[CH2:18](Br)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>O1CCCC1>[C:1]1([C:7]2[CH:12]=[CH:11][C:10]([C:15]([S:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[S:16])=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6348Carbon DisulfideHCID 7498Benzyl BromideHCID 178419618HCID 178419618、化合物

生成物 1

HCID 59819145Benzyl (4-phenyl)dithiobenzoate収率 87%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

In 50 mL of dry tetrahydrofuran, 204 mL of (4-phenyl)phenyl magnesium bromide (a 0.5M tetrahydrofuran solution) was added, and the resulting mixture was stirred and then cooled to 0° C. While keeping 0° C., 7.77 g of carbon disulfide was added over 15 minutes, and the resulting mixture was stirred at 0° C. for 1 hour. Subsequently, 15.86 g of benzyl bromide was added over 15 minutes, and the resulting mixture was stirred at room temperature for 1 hour. After adding 300 mL of ice water, the organic layer was extracted with 500 mL of ethyl acetate. Furthermore, the organic layer was washed with 300 mL of brine and dried over anhydrous magnesium sulfate. The anhydrous magnesium sulfate was removed by filtration, and the residual solvent was then removed. The residue was purified on silica gel (ethyl acetate/hexane solvent) to obtain benzyl (4-phenyl)dithiobenzoate (28.4 g, yield: 87%) (exchange-chain transfer type RAFT agent).

後処理

  1. customWhile keeping 0° C.
  2. stirringthe resulting mixture was stirred at 0° C. for 1 hour
  3. stirringthe resulting mixture was stirred at room temperature for 1 hour
  4. extractionthe organic layer was extracted with 500 mL of ethyl acetate
  5. washFurthermore, the organic layer was washed with 300 mL of brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe anhydrous magnesium sulfate was removed by filtration
  8. customthe residual solvent was then removed
  9. customThe residue was purified on silica gel (ethyl acetate/hexane solvent)

出典と根拠

ORDレコード
ord-047dd168e653488f89b31c8c6fa89d68
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08182975B2

反応ノート

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