反応 #57546

ord-77ce376a03ca4adfa5ba89fc5f893677

反応方程式

C[S-].[Na+]
Sodium thiomethoxide
CN(C)C=O
DMF
BrCc1cccc(Br)c1
1-bromo-3-bromomethyl-benzene
CSCc1cccc(Br)c1
1-bromo-3-methylsulfanylmethyl-benzene
収率 74.8%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to warm to rt
  2. 2
    抽出extracted with EtOAc (3×20 mL)
  3. 3
    乾燥dried with sodium sulfate
  4. 4
    濃縮The solution was concentrated in vacuo
  5. 5
    その他to yield the crude product, which
  6. 6
    その他was then purified via flash chromatography (5% ethyl acetate—hexanes)

実験手順

Sodium thiomethoxide (0.616 g, 8.8 mmol) was added to DMF (8 mL) and cooled to 0° C. To this solution was added 1-bromo-3-bromomethyl-benzene (2 g, 8 mmol). The mixture was allowed to warm to rt and stir for 18 h. The mixture was then poured into cold water (50 mL) and extracted with EtOAc (3×20 mL). The organics were combined and dried with sodium sulfate. The solution was concentrated in vacuo to yield the crude product, which was then purified via flash chromatography (5% ethyl acetate—hexanes) to yield 1.3 g (68.5%) of 1-bromo-3-methylsulfanylmethyl-benzene as a pure product. 1H-NMR (methylene chloride -d2) δ 7.48-7.47 (m, 1H), 7.392 (dt, J=7.9, 1.5 Hz, 1H), 7.28-7.207 (m, 2H), 3.64 (s, 2H), 1.99 (s, 3H); LC-MS RT: 3.70, [M+H]+: 354.1.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07420066B2uspto-grants-2008_09