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Sodium Hydroxide → 2-(4-Chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid

HRID 726148
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HRID 726148 반응식
[Cl:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2([CH2:13][C:14]([O:16]CC)=[O:15])[OH:12].[OH-].[Na+]>C(O)C>[Cl:1][C:2]1[CH:10]=[C:9]([F:11])[CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2([CH2:13][C:14]([OH:16])=[O:15])[OH:12]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 10978626Ethyl 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetate

생성물 1

HCID 110860282-(4-Chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid수율 102.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of ethyl 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetate (14.5 g, 0.05 mol), 1N sodium hydroxide (52 ml) and absolute ethanol (100 ml) was stirred for 18 h at room temperature. The mixture was concentrated in vacuo, diluted with H2O and washed with diethyl ether. The aqueous phase was neutralised with 1.0N hydrochloric acid (52 ml) and extracted with diethyl ether. The diethyl ether extracts were dried over sodium sulphate, filtered and concentrated in vacuo to give 12.5 g (96%) of crude 2-(4-chloro-6-fluoro-1-hydroxy-1-indanyl)acetic acid. This material was used immediately without further purification.

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. additiondiluted with H2O
  3. washwashed with diethyl ether
  4. extractionextracted with diethyl ether
  5. dry with materialThe diethyl ether extracts were dried over sodium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c54cfe93aee64559ac7ef51915a84c96
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05708033

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