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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formaldehyde → Propane, 2,2'-[methylenebis(oxy)]bis[1,1,1,3,3,3-hexafluoro-

HRID 2394988
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인쇄 미리보기

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HRID 2394988 반응식
S(=O)(=O)(O)O.[CH2:6]=[O:7].[CH:8]([OH:17])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10]>C(=O)=O.CC(C)=O>[CH:8]([O:17][CH2:6][O:7][CH:8]([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 135291,1,1,3,3,3-Hexafluoro-2-propanol

생성물 1

HCID 9950185Propane, 2,2'-[methylenebis(oxy)]bis[1,1,1,3,3,3-hexafluoro-

시약·촉매·용매 1

HCID 18522661Acetone cardice용매

실험 절차

A 300 ml reactor, which had been cooled down in dry ice/acetone bath to -20° C., was charged with 111.3 g of fuming sulfuric acid, 9.3 g of paraformaldehyde and 52.8 g of HFIPA, followed by stirring for 20 minutes. After stopping stirring, it was cooled down to room temperature by standing still. With this, the contents were separated into two layers. The organic matter of the upper layer was taken out and then washed with 50 ml of 5% sodium hydrogencarbonate aqueous solution. With this, it was separated into two layers to obtain an organic matter.

후처리

  1. stirringAfter stopping stirring
  2. customWith this, the contents were separated into two layers
  3. washwashed with 50 ml of 5% sodium hydrogencarbonate aqueous solution
  4. customWith this, it was separated into two layers
  5. customto obtain an organic matter

출처 및 근거

ORD 기록
ord-00e2ec1171864691aa16a1c2cff02e3c
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05811596

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