p-Bromobenzenesulfonyl chloride → 4-bromo-N-(tetrahydrofuran-2-ylmethyl)benzenesulfonamide

HRID 1710392노트

반응식

HRID 1710392 반응식
[CH2:1]([NH2:7])[CH:2]1[O:6][CH2:5][CH2:4][CH2:3]1.[Br:8][C:9]1[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1.CCN(C(C)C)C(C)C>ClCCl>[Br:8][C:9]1[CH:14]=[CH:13][C:12]([S:15]([NH:7][CH2:1][CH:2]2[CH2:3][CH2:4][CH2:5][O:6]2)(=[O:17])=[O:16])=[CH:11][CH:10]=1

참가 물질

5

반응물 3

HCID 7396p-Bromobenzenesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 253298Tetrahydrofurfurylamine

생성물 1

HCID 43396864-bromo-N-(tetrahydrofuran-2-ylmethyl)benzenesulfonamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

1.70 ml of commercially available tetrahydrofurfurylamine are dissolved in 45 ml of dry dichloromethane. A solution of 3.83 g of 4-bromo-benzenesulfonyl chloride in 20 ml of dichloromethane are slowly added at room temperature. Subsequently, 5.14 ml of Hünig's base are added and stirring is continued for 1.5 hours. For extraction, the reaction mixture is diluted with 150 ml of dichloromethane and 50 ml of water. The organic layer is dried using Na2SO4, filtered with suction, and concentrated in vacuo. Purification by chromatography on flash silica gel (eluent: dichloromethane/0-5 vol. % ethanol) affords 4.33 g of the title compound as an light yellow oil. ESI-MS: 320.3/322.1 (MH+, 100%:98%). TLC: Rf=0.65 (dichloromethane/ethanol 20:1 parts by volume).

후처리

  1. extractionFor extraction
  2. additionthe reaction mixture is diluted with 150 ml of dichloromethane and 50 ml of water
  3. customThe organic layer is dried
  4. filtrationfiltered with suction
  5. concentrationconcentrated in vacuo
  6. customPurification by chromatography on flash silica gel (eluent: dichloromethane/0-5 vol. % ethanol)

출처 및 근거

ORD 기록
ord-2196b413dc6d4385b2f53b8cff21aab5
출처 데이터셋
uspto-grants-2010_09
특허 번호
US07790710B2

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