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Triethylamine → HCID 22003670, 화합물

HRID 324474
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HRID 324474 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15](=[O:16])[C:10]3[N:11]=[C:12]([CH3:14])[S:13][C:9]=3[CH2:8][CH2:7][C:6]=2[CH:17]=1.BrN1C(=O)CCC1=O.C(N(CC)CC)C>ClCCCl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15](=[O:16])[C:10]3[N:11]=[C:12]([CH3:14])[S:13][C:9]=3[CH:8]=[CH:7][C:6]=2[CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 67184N-bromobutanimideHCID 22003625HCID 22003625, 화합물

생성물 1

HCID 22003670HCID 22003670, 화합물

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

A solution of the product from step (i) (6.05 g) in 1,2-dichloroethane (85 ml) with N-bromosuccinimide (4.1 g) was irradiated with a 500 Watt halogen lamp for 1 h. After cooling to room temperature, triethylamine (7 ml) was added with further stirring for 0.5 hours. The solvents were evaporated under reduced pressure and the residue triturated with acetone, filtered and then further washed with water and then dried under vacuum to leave the subtitle compound as a cream solid.

후처리

  1. customThe solvents were evaporated under reduced pressure
  2. customthe residue triturated with acetone
  3. filtrationfiltered
  4. washfurther washed with water
  5. customdried under vacuum

출처 및 근거

ORD 기록
ord-d10f2582a59744f2b48bac43a44d3950
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06218376B1

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