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1-Butanol → Flurenol-butyl

HRID 898512
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HRID 898512 반응식
[OH:1][C:2]1([C:15]([OH:17])=[O:16])[C:14]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.[CH2:18](O)[CH2:19][CH2:20][CH3:21].S(=O)(=O)(O)O.C(=O)(O)[O-].[Na+]>O.C1(C)C=CC=CC=1>[OH:1][C:2]1([C:15]([O:17][CH2:18][CH2:19][CH2:20][CH3:21])=[O:16])[C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=2[C:9]2[C:14]1=[CH:13][CH:12]=[CH:11][CH:10]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 2631-ButanolHCID 1118Sulfuric AcidHCID 10087FlurenolHCID 516892Sodium Bicarbonate

생성물 1

HCID 40816Flurenol-butyl수율 80%

시약·촉매·용매 2

HCID 962Water용매
HCID 1140
Toluene
용매

실험 절차

To a reactor were added 0.05 mol of 9-hydroxyfluorene-9-carboxlic acid, 0.075 mol of butanol, 40 ml of toluene and 0.4 ml of concentrated sulfuric acid. The reaction was heated to reflux for 6 hrs, while water was separated by a water segregator. At the end of the reaction, the reaction mixture was neutralized with sodium bicarbonate, washed with saturated saline, extracted with ethyl acetate, and dried over anhydrous sodium sulfate. Removing the solvent gave the product with a yield of 80%.

후처리

  1. temperatureThe reaction was heated
  2. customwas separated by a water segregator
  3. customAt the end of the reaction
  4. washwashed with saturated saline
  5. extractionextracted with ethyl acetate
  6. dry with materialdried over anhydrous sodium sulfate
  7. customRemoving the solvent
  8. customgave the product with a yield of 80%

출처 및 근거

ORD 기록
ord-a14efb34ff5e41a38a37228633a5d75f
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07351778B2

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