Diethyl squarate → 3-Ethoxy-4-[(2-hydroxy-6-methylphenyl)amino]-3-cyclobutene-1,2-dione

HRID 357296

반응식

HRID 357296 반응식
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9].[CH3:10][CH2:11][O:12][C:13]1[C:17](=O)[C:15](=[O:16])[C:14]=1[O:19]CC>C(O)C>[CH2:11]([O:12][C:13]1[C:14](=[O:19])[C:15](=[O:16])[C:17]=1[NH:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9])[CH3:10]

참가 물질

4

반응물 2

HCID 123228Diethyl squarateHCID 30141382-Amino-m-cresol

생성물 1

HCID 189374263-Ethoxy-4-[(2-hydroxy-6-methylphenyl)amino]-3-cyclobutene-1,2-dione

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2-amino-3-methylphenol (3.6 g, 29.2 mmol) and diethyl squarate (5 g, 29.4 mmol) in dry ethanol (80 mL) was heated to reflux for two days, then allowed to stand at room temperature for 48 hours. The reaction mixture was concentrated under reduced pressure and the resulting residue was suspended in ethyl acetate (50 mL). Hexane (50 mL) was added to produce a slurry, which was filtered, and rinsed with three portions of hexane:ethyl acetate (1:1). The resulting solid was suspended in dichloromethane (200 mL) and methanol (20 mL), stirred at room temperature for 30 minutes, and filtered. The precipitate was suspended in hot dichloromethane, filtered hot, and dried to give 3-ethoxy-4-(2-hydroxy-6-methylphenylamino)-cyclobut-3-ene-1,2-dione, 1.56 g (6.3 mmol, 22%).

후처리

  1. temperatureto reflux for two days
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additionHexane (50 mL) was added
  4. customto produce a slurry, which
  5. filtrationwas filtered
  6. washrinsed with three portions of hexane:ethyl acetate (1:1)
  7. filtrationfiltered
  8. filtrationfiltered hot
  9. customdried

출처 및 근거

ORD 기록
ord-ca6c9425068e44fb973eae46052db046
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05840764

연결된 노트

불러오는 중…