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Water → (alphaRS)-Cyano-3-benzoylbenzyl alcohol

HRID 358117
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HRID 358117 반응식
[C:1]([C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH:12]=[O:13])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.[C-:18]#[N:19].[Na+].S(=O)(=O)(O)O>O1CCOCC1>[C:18]([CH:12]([OH:13])[C:11]1[CH:14]=[CH:15][CH:16]=[C:9]([C:1](=[O:8])[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:10]=1)#[N:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 1118Sulfuric AcidHCID 8929Sodium CyanideHCID 130201683-Benzoylbenzaldehyde

생성물 1

HCID 12783740(alphaRS)-Cyano-3-benzoylbenzyl alcohol

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

3-Benzoylbenzaldehyde (1.0 g) in dioxan (5 ml) was treated with water (2.5 ml) and sodium cyanide (0.5 g). The whole was cooled below 15° C. and 40% sulphuric acid (1.4 ml) added dropwise (care being taken to ensure that this temperature was not exceeded). Stirring was continued for 1 hour when water (30 ml) was added and the product extracted with methylene chloride and washed with water, saturated NaCl, dried over Na2SO4 and evaporated.

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후처리

  1. temperatureThe whole was cooled below 15° C.
  2. extractionthe product extracted with methylene chloride
  3. washwashed with water, saturated NaCl
  4. dry with materialdried over Na2SO4
  5. customevaporated

출처 및 근거

ORD 기록
ord-34e9d3e29a634511921d6d36ba982ada
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04464391

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