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Hydrochloric Acid → 6-Hydroxy-2-phenylchroman-4-one Oxime

HRID 31248
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HRID 31248 반응식
[OH-:1].[Na+].[OH:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[O:10][CH:9]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:8][C:7]2=O.Cl.[NH2:22]O.Cl>C(O)C.O>[OH:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[O:10][CH:9]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH2:8][C:7]2=[N:22][OH:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium Hydroxide2회HCID 443297Hydroxyamine hydrochloride2회HCID 27345806-Hydroxyflavanone

생성물 1

HCID 734147306-Hydroxy-2-phenylchroman-4-one Oxime

시약·촉매·용매 2

HCID 702Ethanol용매
HCID 962
Water
용매
2회

실험 절차

Sodium hydroxide (122 mg) was added into a cooled solution of 6-hydroxyflavanone (2 g) and hydroxylamine hydrochloride (900 mg) in ethanol (5 ml) and water (2 ml). Resulting mixture was refluxed for 6 hours and hydroxylamine hydrochloride (450 mg) and sodium hydroxide (61 mg) were added after every 45 min. After cooling into room temperature water (23 ml) and concentrated hydrochloric acid (5.6 ml) were added into the mixture. Precipitate was filtered, washed with water and dried in vacuum. 1H-NMR (400 MHz, d6-DMSO): 11.3 (s, 1H), 9.11 (s, 1H), 7.50-7.48 (m, 2H), 7.43-7.33 (m, 3H), 7.21 (d, 1H, J 2.9 Hz), 6.80 (d, 1H, J 8.8 Hz), 6.72 (dd, 1H, J 2.9, 8.8 Hz), 5.07 (dd, 1H, J 3.2, 11.9 Hz), 3.28 (dd, 1H, J 3.2, 17.1 Hz), 2.64 (dd, 1H, J 11.9,17.1 Hz).

후처리

  1. customResulting mixture
  2. temperaturewas refluxed for 6 hours
  3. additionwere added into the mixture
  4. filtrationPrecipitate was filtered
  5. washwashed with water
  6. customdried in vacuum

출처 및 근거

ORD 기록
ord-68152485343046639c761c00120b42fd
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07425568B2

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