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Sodium Hydroxide → Cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide

HRID 2428135
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HRID 2428135 반응식
[OH-].[Na+].C([SiH2][O:8][C:9](C)(C)[C:10]1[CH:11]=[C:12]([CH:20]=[CH:21][C:22]=1[Cl:23])[CH2:13][NH:14][C:15]([CH:17]1[CH2:19][CH2:18]1)=[O:16])(C)(C)C>CO>[Cl:23][C:22]1[CH:21]=[CH:20][C:12]([CH2:13][NH:14][C:15]([CH:17]2[CH2:18][CH2:19]2)=[O:16])=[CH:11][C:10]=1[CH2:9][OH:8]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 137328721Cyclopropanecarboxylic Acid 3-(tert-butyl-dimethyl-silanyloxymethyl)-4-chloro-benzylamide

생성물 1

HCID 67148310Cyclopropanecarboxylic acid 4-chloro-3-hydroxymethyl-benzylamide수율 84.2%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
80 °C

실험 절차

Aq. 1M NaOH (111 mL) was added to a sol. of cyclopropanecarboxylic acid 3-(tert-butyl-dimethyl-silanyloxymethyl)-4-chloro-benzylamide (6.10 g, 17.2 mmol) in MeOH (222 mL). The mixture was heated to 80° C., and stirred at this temperature for 30 min. The mixture was allowed to cool to rt, and the solvents were partially removed under reduced pressure. The aq. residue was diluted with water, and was extracted with EtOAc (3×). The combined org. extracts were washed with brine, dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC(CH2Cl2→MeOH/CH2Cl2 1:9) yielded the title compound (3.47 g, 84%). LC-MS: tR=0.71 min; ES+: 281.31.

후처리

  1. temperatureto cool to rt
  2. customthe solvents were partially removed under reduced pressure
  3. additionThe aq. residue was diluted with water
  4. extractionwas extracted with EtOAc (3×)
  5. washextracts were washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customthe solvents were removed under reduced pressure
  9. customPurification of the crude by FC(CH2Cl2→MeOH/CH2Cl2 1:9)

출처 및 근거

ORD 기록
ord-a08dc26b278d49b4b12496d5250d7150
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968720B2

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