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Diphenylmethane → HCID 178506622, 화합물

HRID 1736954
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HRID 1736954 반응식
[C:1]1([CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O(C(CC)(C)C)[K:15].C([Li])CCC>CCCCCC>[C:1]1([CH:7]([K:15])[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7580DiphenylmethaneHCID 178418339ButyllithiumHCID 178447184HCID 178447184, 화합물

생성물 1

HCID 178506622HCID 178506622, 화합물

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

To a solution of 18.3 g (109 mmol) of diphenylmethane in 400 mL of hexane were added 11.99 g (109 mmol) of potassium t-amylate. To the resulting pale yellow solution were added 68.75 mL of 1.60M (110 mmol) butyl lithium. The thick, bright orange slurry was stirred overnight. The solids were collected on a filter, washed three times with 100 mL, then twice with 50 mL of hexane, then dried under reduced pressure. The yield of bright orange powder was 18.23 g, 81.2 percent.

후처리

  1. customThe solids were collected on a filter
  2. washwashed three times with 100 mL
  3. dry with materialtwice with 50 mL of hexane, then dried under reduced pressure

출처 및 근거

ORD 기록
ord-e65ee5d3d8b64351b0a2c46207024d05
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05541349

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