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Sulfuric Acid → 2-Chloro-1-[3,4-bis(acetyloxy)phenyl]ethanone

HRID 4114
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HRID 4114 반응식
[Cl:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[C:7]([OH:12])[CH:6]=1)=[O:4].S(=O)(=O)(O)O>C(OC(=O)C)(=O)C>[Cl:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][C:3](=[O:4])[CH3:2])=[C:7]([O:12][C:8](=[O:11])[CH3:7])[CH:6]=1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 668342-Chloro-3',4'-dihydroxyacetophenone

생성물 1

HCID 137646832-Chloro-1-[3,4-bis(acetyloxy)phenyl]ethanone

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

A suspension of α-chloro-3',4'-dihydroxyacetophenone (9.33 g, 0.05 mole) in 78 ml of acetic anhydride was treated with 0.1 ml of concentrated sulfuric acid and stirred for 1.5 hours under an argon atmosphere. Initially, the reaction temperature rose to 40° C. and the starting material completely dissolved yielding a clear, colorless solution which was poured onto approximately 300 g of crushed ice. After standing for one hour, the crystallized product was filtered, washed with cold water (200 ml) and dried in vacuo overnight at room temperature; yield: 11.5 g.

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후처리

  1. customrose to 40° C.
  2. dissolutionthe starting material completely dissolved
  3. customyielding a clear, colorless solution which
  4. waitAfter standing for one hour
  5. filtrationthe crystallized product was filtered
  6. washwashed with cold water (200 ml)
  7. customdried in vacuo overnight at room temperature

출처 및 근거

ORD 기록
ord-c98143d1d5664d11907a5d25e56ab78d
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04723002

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