Benzaldehyde → 2-Phenyl-2H-pyran-4(3H)-one

HRID 650697

반응식

HRID 650697 반응식
ClCCl.[CH:4](=[O:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.CO[CH:14]=[CH:15][C:16]([O:18][Si](C)(C)C)=[CH2:17]>FC(F)(F)C(O)=O.N1C=CC=CC=1.O>[C:5]1([CH:4]2[CH2:17][C:16](=[O:18])[CH:15]=[CH:14][O:11]2)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

참가 물질

7

반응물 3

HCID 240BenzaldehydeHCID 6344DichloromethaneHCID 1010511-Methoxy-3-trimethylsilyloxy-1,3-butadiene

생성물 1

HCID 5690202-Phenyl-2H-pyran-4(3H)-one수율 93%

시약·촉매·용매 3

HCID 1049Pyridine촉매HCID 6422Trifluoroacetic acid촉매HCID 962Water용매

실험 절차

To a round flask of 5 ml having a magnet stirrer put therein, 19.1 mg (0.01 mmol) of the catalyst (tetrahydrate) obtained in Example 8 and 1 ml of dichloromethane were added for dissolution, then benzaldehyde (10 μl, 0.1 mmol) and 1-methoxy-3-trimethylsilyloxy-1,3-butadiene (purity: 90%, 30.0 μl, 0.150 mmol) were added thereto, and the reaction was carried out at room temperature for 24 hours. After the reaction had been completed, two drops of trifluoroacetic acid was added by a microsyringe, three drops of pyridine was added by a microsyringe, and 1 ml of water was added. Successively, extraction with dichloromethane, drying over anhydrous magnesium sulfate, concentration and purification by preparative silica gel column chromatography (hexane/ethyl acetate=4/1) were carried out to obtain 16.1 mg of the desired compound (R)-2-phenyl-2,3-dihydro-4H-pyran-4-one. As a result of analysis, the yield was 93% and the optical purity was 19% (R).

후처리

  1. customTo a round flask of 5 ml having
  2. customa magnet stirrer put
  3. additionwere added for dissolution
  4. additionwas added
  5. extractionSuccessively, extraction with dichloromethane
  6. dry with materialdrying over anhydrous magnesium sulfate, concentration and purification by preparative silica gel column chromatography (hexane/ethyl acetate=4/1)

출처 및 근거

ORD 기록
ord-6d0477b2e22a4c7bbae98a7f9dc9bc0a
출처 데이터셋
uspto-grants-2001_08
특허 번호
US06274745B1

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