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Hydrochloric Acid → HCID 86648130, 화합물

HRID 2388242
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HRID 2388242 반응식
[OH-:1].[Na+].Cl.[NH2:4]O.[CH2:6]([O:8][C:9](=[O:22])[C:10](=[O:21])[CH:11]([CH3:20])[C:12]([CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)=O)[CH3:7].Cl>O.C(OCC)(=O)C>[CH2:6]([O:8][C:9](=[O:22])[C:10](=[O:21])[CH:11]([CH3:20])[C:12]([CH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)=[N:4][OH:1])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 67529552HCID 67529552, 화합물

생성물 1

HCID 86648130HCID 86648130, 화합물수율 56.5%

시약·촉매·용매 2

HCID 962Water용매
HCID 8857
Ethyl Acetate
용매

실험 절차

Sodium hydroxide (0.99 g, 24.7 mmol) was dissolved in 5.5 mL of water. Hydroxylamine hydrochloride (1.71 g, 24.7 mmol) was added and the reaction mixture was stirred until complete dissolution was achieved. 4-Cyclohexyl-3-methyl-2,4-dioxo-butyric acid ethyl ester (5.15 g, 21.5 mmol) was added and the resulting mixture was stirred at ambient temperature for 16 h. Ethyl acetate (20 mL) and 1M hydrochloric acid (10 mL) was added, and the aqueous layer was extracted with additional ethyl acetate (4×20 mL). The organic layers were combined, dried over MgSO4 and concentrated. The crude oil was purified by chromatography (0-30% EtOAc/hexanes) to give 3.1 g of the title compound. MS: (+) m/z 256.39 (M+1).

후처리

  1. stirringthe resulting mixture was stirred at ambient temperature for 16 h
  2. extractionthe aqueous layer was extracted with additional ethyl acetate (4×20 mL)
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated
  5. customThe crude oil was purified by chromatography (0-30% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-e6db7fe6412e40b784d2dc1f1c7a4dc0
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08269008B2

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