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Sodium Hydroxide → HCID 19004497, 화합물

HRID 2225809
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HRID 2225809 반응식
C[O:2][C:3](=[O:25])[C:4](=[O:24])[C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][C:13]([NH:15][CH:16]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)=[O:14])=[CH:7][CH:6]=1.[OH-].[Na+]>CO>[CH:16]1([NH:15][C:13](=[O:14])[CH2:12][O:11][C:8]2[CH:7]=[CH:6][C:5]([C:4](=[O:24])[C:3]([OH:25])=[O:2])=[CH:10][CH:9]=2)[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23]1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 54288573HCID 54288573, 화합물

생성물 1

HCID 19004497HCID 19004497, 화합물수율 21.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 4-[2-(cyclooctylamino)-2-oxoethoxy]-alpha-oxobenzeneacetic acid methyl ester (0.4 g) in methanol (40 mL) was treated with 1N sodium hydroxide solution (1.3 mL), and the mixture was stirred at room temperature for 15 minutes. After the solvents were evaporated under reduced pressure, water (20 mL) was added and the solution was acidified with 3N hydrochloric acid, then the aqueous layer was extracted with a mixture of dichloromethane-tetrahydrofuran (30 mL; 2:1). The organic layer was dried (MgSO4), evaporated and the resulting oil was crystallized from diethyl ether-hexane to yield 0.084 g of 4-[2-(cyclooctylamino)-2-oxoethoxy]-alpha-oxobenzeneacetic acid, mp 139°-140 ° C.

후처리

  1. customAfter the solvents were evaporated under reduced pressure, water (20 mL)
  2. additionwas added
  3. extractionthe aqueous layer was extracted with a mixture of dichloromethane-tetrahydrofuran (30 mL; 2:1)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. customevaporated
  6. customthe resulting oil was crystallized from diethyl ether-hexane

출처 및 근거

ORD 기록
ord-f2f20167ecbc496487137a17998ae789
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05344843

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