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Aluminium lithium hydride → (2-(2-(Dimethylamino)ethylamino)-3-fluorophenyl)methanol

HRID 1695934
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HRID 1695934 반응식
[CH3:1][N:2]([CH3:17])[CH2:3][CH2:4][NH:5][C:6]1[C:15]([F:16])=[CH:14][CH:13]=[CH:12][C:7]=1[C:8](OC)=[O:9].[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC.[F-].[Na+].O>[CH3:1][N:2]([CH3:17])[CH2:3][CH2:4][NH:5][C:6]1[C:15]([F:16])=[CH:14][CH:13]=[CH:12][C:7]=1[CH2:8][OH:9]
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참가 물질

6

반응물 2

HCID 21226445Aluminium lithium hydride2회HCID 57774398Methyl 2-(2-(dimethylamino)ethylamino)-3-fluorobenzoate

생성물 1

HCID 57774489(2-(2-(Dimethylamino)ethylamino)-3-fluorophenyl)methanol수율 82.1%

시약·촉매·용매 3

HCID 962Water용매HCID 3283Diethyl Ether용매2회
HCID 5235
Sodium Fluoride
용매

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온도
0 °C

실험 절차

A solution of methyl 2-(2-(dimethylamino)ethylamino)-3-fluorobenzoate (749 mg, 3.117 mmol) in Et2O (30 mL) at −20° C. was treated with LAH (166 mg, 4.374 mmol). After 1.5 hours, additional LAH (15 mg, 0.3952 mmol) was added and the reaction was warmed to 0° C. After 1 hour at 0° C., the reaction was diluted with Et2O (70 mL) and NaF and water were added with vigorous stirring until the reaction was quenched and a white ppt formed. The clear solution was decanted and evaporated under vacuum. The crude material was purified on a 12 g ISCO redisep column (0-10% MeOH in CH2Cl2 as eluent) to yield 543 mg (82%) of (2-(2-(dimethylamino)ethylamino)-3-fluorophenyl)methanol as a clear oil. FIA: 213.08 (M+1).

후처리

  1. waitAfter 1 hour at 0° C.
  2. additionwere added
  3. customwas quenched
  4. customa white ppt formed
  5. customThe clear solution was decanted
  6. customevaporated under vacuum
  7. customThe crude material was purified on a 12 g ISCO redisep column (0-10% MeOH in CH2Cl2 as eluent)

출처 및 근거

ORD 기록
ord-003fd58c29cb4a338eb4198b9f86af31
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163737B2

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