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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetone → 6-(Hydroxymethyl)-2,3-dihydro-1H-inden-1-one

HRID 2377240
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HRID 2377240 반응식
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4](S(O)(=O)=O)=[CH:3][CH:2]=1.C(=O)([O-])[O-:13].[K+].[K+].[CH3:18][C:19]([CH3:21])=[O:20]>O>[OH:13][CH2:11][C:1]1[CH:2]=[C:21]2[C:4]([CH2:3][CH2:18][C:19]2=[O:20])=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 6101p-Toluenesulfonic acidHCID 11430Potassium Carbonate

생성물 1

HCID 211357856-(Hydroxymethyl)-2,3-dihydro-1H-inden-1-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of Example 28 (8.0 g, 38.7 mmol) and p-toluenesulfonic acid (7.4 g, 38.7 mmol) in a mixture of water (20 mL) and acetone (85 mL) was heated to reflux for about 1 hour. The mixture was concentrated under vacuum, diluted with water, and neutralized by careful addition of potassium carbonate (2.7 g, 19.4 mmol). The precipitate was collected by filtration, washed with minimal water and diethyl ether, and dried under vacuum to provide the desired product. MS (DCI-NH3): m/z 180 (M+NH4)+.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for about 1 hour
  3. concentrationThe mixture was concentrated under vacuum
  4. additiondiluted with water
  5. filtrationThe precipitate was collected by filtration
  6. washwashed with minimal water and diethyl ether
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-ddd5005a16b14830a0335f61a1857d1a
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07468371B2

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