Hydrochloric Acid → 2-Methoxy-5,8-dihydronaphthalene-1,4-diol

HRID 2260359노트

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HRID 2260359 반응식
[CH3:1][O:2][C:3]1[C:4](=[O:14])[CH:5]2[CH:10]([C:11](=[O:13])[CH:12]=1)[CH2:9][CH:8]=[CH:7][CH2:6]2.N#N.C([O-])([O-])=O.[K+].[K+].Cl>CO>[CH3:1][O:2][C:3]1[CH:12]=[C:11]([OH:13])[C:10]2[CH2:9][CH:8]=[CH:7][CH2:6][C:5]=2[C:4]=1[OH:14]

참가 물질

6

실험 절차

A solution of 2-methoxy-4a,5,8,8a-tetrahydronaphthalene-1,4-dione (55, 542 mg, 2.82 mmol) in MeOH (50 mL) was purged with a stream of N2 for 5 min with stirring at rt. With continued N2 purging, solid K2CO3 (390 mg, 2.82 mmol, Baker) was added to the stirred solution. The solution immediately turned yellow. The reaction was allowed to stir for 15 min at rt under N2, after which it was brown. To this there was added a dilute HCl solution (10% concd HCl, 90% H2O, 50 mL) in one portion. The MeOH was removed in vacuo to give a colorless suspension. The suspended material was collected by filtration, washed with a dilute acid solution (as above, 4×6 mL) and dried in vacuo to yield a fluffy colorless solid (444 mg, 82%, pure by 1H NMR analysis (unstable on TLC)); mp 142.5°-144° C. (confirmed), lit. (Cavill et al., supra) 123°-124° C. (benzene/petroleum ether); 1H NMR (CDCl3) δ2.21 (m, 2H), 3.32 (m, 2H), 3.84 (s, 3H), 4.25 (s, 1H), 5.25 (s, 1H), 5.90 (m, 2H), 6.36 (s, 1H).

후처리

  1. stirringto stir for 15 min at rt under N2
  2. customThe MeOH was removed in vacuo
  3. customto give a colorless suspension
  4. filtrationThe suspended material was collected by filtration
  5. washwashed with a dilute acid solution (as above, 4×6 mL)
  6. customdried in vacuo
  7. customto yield a fluffy colorless solid (444 mg, 82%, pure by 1H NMR analysis (unstable on TLC))

출처 및 근거

ORD 기록
ord-7d8d6eb0ec39442983204f7829f9b820
출처 데이터셋
uspto-grants-1995_12
특허 번호
US05476933

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