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Hydrochloric Acid → 1-(4-Amino-3,5-dimethyl-phenyl)-2,2,2-trifluoro-1-(4-fluorophenyl)-ethanol

HRID 1917053
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HRID 1917053 반응식
[F:1][C:2]([F:30])([F:29])[C:3]([C:22]1[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=1)([C:5]1[CH:10]=[C:9]([CH3:11])[C:8]([N:12]([Si](C)(C)C)[Si](C)(C)C)=[C:7]([CH3:21])[CH:6]=1)[OH:4].Cl.[OH-].[Na+]>O1CCCC1>[NH2:12][C:8]1[C:9]([CH3:11])=[CH:10][C:5]([C:3]([C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)([OH:4])[C:2]([F:1])([F:29])[F:30])=[CH:6][C:7]=1[CH3:21]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 594978232,2,2-Trifluoro-1-(4-fluoro-phenyl)-1-[4-(1,1,1,3,3,3-hexamethyl disilazan-2-yl)-3,5-dimethyl-phenyl]-ethanol

생성물 1

HCID 594978191-(4-Amino-3,5-dimethyl-phenyl)-2,2,2-trifluoro-1-(4-fluorophenyl)-ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
20 °C

실험 절차

To a solution of 2,2,2-trifluoro-1-(4-fluoro-phenyl)-1-[4-(1,1,1,3,3,3-hexamethyl disilazan-2-yl)-3,5-dimethyl-phenyl]-ethanol (Example I2) (5 mmol) in tetrahydrofuran (15 ml) was added aqueous hydrochloric acid (concentrated) (1 ml) at 20° C. The reaction mixture was stirred at 20° C. for 15 hours. The reaction mixture was neutralized by addition of aqueous sodium hydroxide (4M). The mixture was extracted with diethyl ether. The organic phase was dried over sodium sulfate, filtered through a plug of silica gel and concentrated. The residue was triturated with heptane and a small amount of diethyl ether, then filtered and dried. The title compound was isolated as off-white crystals.

후처리

  1. customat 20° C
  2. extractionThe mixture was extracted with diethyl ether
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. filtrationfiltered through a plug of silica gel
  5. concentrationconcentrated
  6. customThe residue was triturated with heptane
  7. filtrationa small amount of diethyl ether, then filtered
  8. customdried

출처 및 근거

ORD 기록
ord-73cadd65aa904144928d79a4b7175d74
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08618173B2

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