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Water → HCID 59637734, 화합물

HRID 1892018
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HRID 1892018 반응식
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][C:11]#[CH:12])=[O:8].[K].[C:14]1(=[O:24])[NH:18][C:17](=[O:19])[C:16]2=[CH:20][CH:21]=[CH:22][CH:23]=[C:15]12.C(Cl)(Cl)Cl.O>CN(C=O)C>[C:14]1(=[O:24])[N:18]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH2:10][C:11]#[CH:12])=[O:8])[C:17](=[O:19])[C:16]2=[CH:20][CH:21]=[CH:22][CH:23]=[C:15]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6212ChloroformHCID 24194345Phthalimide potassium saltHCID 59637736HCID 59637736, 화합물

생성물 1

HCID 59637734HCID 59637734, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Prop-2-ynyl 6-bromohexanoate (0.606 g, 2 mmol, 1 eq.) was added to a solution of phthalimide potassium salt (0.441 g, 2.4 mmol, 1.2 eq.) in 50 mL of DMF and stirred overnight under argon. CHCl3 was added to the solution flask and was transferred to a separatory funnel containing water. The aqueous layer was separated and twice extracted with CHCl3. The combined organic layers were twice extracted with water then the solvent was removed on a rotary evaporator. Remaining solvent was removed under high vacuum overnight to yield a brown oil.

후처리

  1. customwas transferred to a separatory funnel
  2. customThe aqueous layer was separated
  3. extractiontwice extracted with CHCl3
  4. extractionThe combined organic layers were twice extracted with water
  5. customthe solvent was removed on a rotary evaporator
  6. customRemaining solvent was removed under high vacuum overnight
  7. customto yield a brown oil

출처 및 근거

ORD 기록
ord-2e107c983d4b4d87bf164668b2e1244f
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507572B2

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