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Sodium Hydroxide → HCID 21949787, 화합물

HRID 558301
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HRID 558301 반응식
[OH-].[Na+].C[O:4][C:5](=[O:25])[CH2:6][N:7]1[C:11]([CH2:12][CH3:13])=[C:10]([O:14][C:15]2[CH:20]=[C:19]([Cl:21])[CH:18]=[C:17]([Cl:22])[CH:16]=2)[C:9]([CH2:23][CH3:24])=[N:8]1>O1CCCC1>[Cl:22][C:17]1[CH:16]=[C:15]([CH:20]=[C:19]([Cl:21])[CH:18]=1)[O:14][C:10]1[C:9]([CH2:23][CH3:24])=[N:8][N:7]([CH2:6][C:5]([OH:25])=[O:4])[C:11]=1[CH2:12][CH3:13]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 10291825HCID 10291825, 화합물

생성물 1

HCID 21949787HCID 21949787, 화합물수율 78%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Aqueous sodium hydroxide solution (1N, 6.2 ml, 6.2 mmol) was added dropwise to a stirred solution of the ester (2 g, 5.6 mmol) of Example 9 in tetrahydrofuran (20 ml) at 0° C. After 1 hour the solvent was removed under reduced pressure and aqueous hydrochloric acid (20 ml) was added with vigorous stirring. The resulting white precipitate was collected by filtration, washed with ether (3×30 ml) and dried in a vacuum pistol at 60° C./10 mmHg to afford the title compound as a white solid (1.5 g), m.p. 157-158° C.

후처리

  1. customAfter 1 hour the solvent was removed under reduced pressure and aqueous hydrochloric acid (20 ml)
  2. additionwas added with vigorous stirring
  3. filtrationThe resulting white precipitate was collected by filtration
  4. washwashed with ether (3×30 ml)
  5. customdried in a vacuum pistol at 60° C./10 mmHg

출처 및 근거

ORD 기록
ord-efb0a3a7f8fa459a98e46e7fba19ebc4
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063044B2

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