2-Thiopheneglyoxylic acid → 2-Hydroxyimino(thien-2-yl)acetic acid

HRID 1707168

반응식

HRID 1707168 반응식
Cl.[NH2:2][OH:3].C(=O)(O)[O-].[Na+].[S:9]1[CH:13]=[CH:12][CH:11]=[C:10]1[C:14](=O)[C:15]([OH:17])=[O:16]>O>[OH:3][N:2]=[C:14]([C:10]1[S:9][CH:13]=[CH:12][CH:11]=1)[C:15]([OH:17])=[O:16]

참가 물질

5

실험 절차

A cooled solution of hydroxylamine hydrochloride (0.884 g) and sodium bicarbonate (1.08 g) in water (20 ml.) was added to a cooled (0°) solution of thien-2-yl-glyoxylic acid (2.0 g) and sodium bicarbonate (1.08 g) in water (20 ml.). After two days at 20° the solution was extracted with ether, cooled and acidified with concentrated hydrochloric acid. The resulting white solid was filtered off (0.564 g) and the filtrate was then thoroughly extracted with ether. The combined extracts were washed with brine, dried and concentrated. The solid residue was triturated with benzene to give the oxime (syn-isomer) (1.05 g; 51%), m.p. 132°, λmax. (ethanol) 284 nm (ε 9,500), λmax. (Nujol) 2590 and 1706 (CO2H) and 1655 cm-1 (C=N), τ (DMSO-d6), -2.5 to -0.5 (broad multiplet; N--OH and COOH), 2.36 (multiplet; thienyl C-5 H) and 2.82 (multiplet; thienyl C-3 H and C-4 H).

후처리

  1. extractionAfter two days at 20° the solution was extracted with ether
  2. temperaturecooled
  3. filtrationThe resulting white solid was filtered off (0.564 g)
  4. extractionthe filtrate was then thoroughly extracted with ether
  5. washThe combined extracts were washed with brine
  6. customdried
  7. concentrationconcentrated
  8. customThe solid residue was triturated with benzene

출처 및 근거

ORD 기록
ord-4f4be94a626e4402a3d47f22384adabd
출처 데이터셋
uspto-grants-1980_06
특허 번호
US04209616

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