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Sodium Chloride → 4-Amino-2(alpha-hydroxybenzyl)-2'-methoxymethoxy-6'-methoxy-biphenyl

HRID 1358116
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HRID 1358116 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=2[O:16][CH2:17][O:18][CH3:19])=[C:4]([C:20](=[O:27])[C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:3]=1.[BH4-].[Na+].C(Cl)(Cl)Cl.[Na+].[Cl-]>C(O)C>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=2[O:16][CH2:17][O:18][CH3:19])=[C:4]([CH:20]([OH:27])[C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 5234Sodium ChlorideHCID 6212ChloroformHCID 4311764Sodium borohydrideHCID 181885574-Amino-2-benzoyl-2'-methoxymethoxy-6'-methoxy-biphenyl

생성물 1

HCID 181891954-Amino-2(alpha-hydroxybenzyl)-2'-methoxymethoxy-6'-methoxy-biphenyl수율 80%

시약·촉매·용매 1

HCID 702
Ethanol
용매

실험 절차

The compound of Example 5D (4.84, 13.31 mmol) in ethanol (45 mL) was heated at 65° C. with NaBH4(2.03 g, 53.42 mmol). After 1 hour Chloroform and aqueous NaCl was added. The organic phase was separated, washed with aqueous KHCO3, dried (Na2SO4), filtered and the solvent removed under reduced pressure to provide the titled compound (3.844 g, 80%).

후처리

  1. customThe organic phase was separated
  2. washwashed with aqueous KHCO3
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-cac13647593b46009d3c748982c29a73
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06593480B2

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