反応 #8497

ord-fc08a00bc9a040b3a45a8e40ce7d7458

反応方程式

Clc1cc(Cl)cc(Cl)c1
1,3,5-trichlorobenzene
[Na+].[OH-]
sodium hydroxide
CC(C)(C)S
tert-butylmercaptan
CC(C)(Cc1cc(Cl)cc(Cl)c1)SC(C)(C)Cc1cc(Cl)cc(Cl)c1
( 4 )
収率 19.0%
CC(C)(Cc1cc(Cl)cc(Cl)c1)SC(C)(C)Cc1cc(Cl)cc(Cl)c1
3,5-Dichlorophenyl-tert-butylsulfide
収率 19.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was refluxed at 140° C. for 6.5 hours
  2. 2
    抽出extracted with ethylacetate
  3. 3
    洗浄washed with water
  4. 4
    乾燥dried over sodium sulphate
  5. 5
    ろ過filtrated
  6. 6
    濃縮concentrated under reduced pressure
  7. 7
    その他The obtained residue was chromatographed twice on silica gel (SiO2 15 g, elution: n-hexane)

実験手順

To a solution of 4N sodium hydroxide (0.8 ml) was added tert-butylmercaptan (0.406 ml). The mixture was stirred for 15 minutes at room temperature. Tetra n-butylammonium bromide (322 mg, 1 mmol) and 1,3,5-trichlorobenzene (1) (1.8 g, 10 mmol) were added thereto. The reaction mixture was refluxed at 140° C. for 6.5 hours. The reaction mixture was poured into ice-water, extracted with ethylacetate, washed with water, dried over sodium sulphate, filtrated and concentrated under reduced pressure. The obtained residue was chromatographed twice on silica gel (SiO2 15 g, elution: n-hexane) to yield the objective (4) (138 mg). Yield 19%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07087764B2uspto-grants-2006_08