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Hydrochloric Acid → 4-(4-Bromo-benzyl)-2-phenyl morpholine

HRID 737068
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인쇄 미리보기

반응식

HRID 737068 반응식
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.Cl.[C:11]1([CH:17]2[O:22][CH2:21][CH2:20][NH:19][CH2:18]2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C1COCC1>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][N:19]2[CH2:20][CH2:21][O:22][CH:17]([C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:18]2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 707414-BromobenzaldehydeHCID 911012-Phenylmorpholine

생성물 1

HCID 578495044-(4-Bromo-benzyl)-2-phenyl morpholine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

429 mg of 4-Bromobenzaldehyde was dissolved in 6 mL of THF and 386 mg of the HCl salt of 2-Phenylmorpholine (Array) and 1.15 g of MP-BH(OAc)3 (2.77 mmol/g) was added. The reaction was agitated on an orbital shaker overnight at room temperature. The reaction was filtered and the resin washed several times with dichloromethane. The filtrate was concentrated and purified by flash chromatography. Yield: 281 mg.

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후처리

  1. filtrationThe reaction was filtered
  2. washthe resin washed several times with dichloromethane
  3. concentrationThe filtrate was concentrated
  4. custompurified by flash chromatography

출처 및 근거

ORD 기록
ord-715723e31ae746169d3cfd6a7a320f4e
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07595397B2

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