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1-Bromohexane → HCID 59467510, 화합물

HRID 1715679
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HRID 1715679 반응식
[H-].[Na+].[Cl:3][C:4]1[C:9]([NH:10][C:11](=[O:18])[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:8][CH:7]=[CH:6][N:5]=1.Br[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25]>O1CCCC1>[Cl:3][C:4]1[C:9]([N:10]([CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])[C:11](=[O:18])[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:8][CH:7]=[CH:6][N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 81011-BromohexaneHCID 24758Sodium hydrideHCID 836063HCID 836063, 화합물

생성물 1

HCID 59467510HCID 59467510, 화합물수율 58%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

0.63 g sodium hydride (NaH) (26 mmol) and 50 mL tetrahydrofuran (THF) were added in an ice bath with stirring. 3.01 g N-(2-chloro-pyridin-3-yl)-benzamide (13 mmol) and 40 mL THF were then added and reacted for 30 min. Next, 3.28 g 1-bromo-hexane (20 mmol) was added and reacted for 24 hr. After cooling to room temperature, the reaction was quenched by water. After extraction three times by ethyl acetate, removal of water by magnesium sulphate (MgSO4), concentration, and purification by column, 2.39 g white solid was obtained, with a yield of 58%.

후처리

  1. customreacted for 30 min
  2. customreacted for 24 hr
  3. customthe reaction was quenched by water
  4. extractionAfter extraction three times
  5. customby ethyl acetate, removal of water
  6. concentrationby magnesium sulphate (MgSO4), concentration, and purification by column

출처 및 근거

ORD 기록
ord-c9120b3d46c447e6942f84155d4127c9
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07799918B2

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