Ethanol → HCID 58540128, 화합물

HRID 1907795노트

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HRID 1907795 반응식
[CH3:1][C:2]1([CH3:16])[CH2:14][C:5]2[S:6][C:7]([C:9]([O:11]CC)=[O:10])=[CH:8][C:4]=2[C:3]1=[O:15].C1COCC1.C(O)C.[OH-].[Li+]>O>[CH3:1][C:2]1([CH3:16])[CH2:14][C:5]2[S:6][C:7]([C:9]([OH:11])=[O:10])=[CH:8][C:4]=2[C:3]1=[O:15]

참가 물질

6

반응물 4

HCID 702EthanolHCID 3939Lithium HydroxideHCID 8028TetrahydrofuranHCID 58539987Ethyl 5,5-Dimethyl-4-oxo-5,6-dihydro-4H-cyclopenta[b]thiophene-2-carboxylate

생성물 1

HCID 58540128HCID 58540128, 화합물수율 106.8%

시약·촉매·용매 1

HCID 962Water용매

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온도
50 °C

실험 절차

A 50-mL single-neck round-bottomed flask equipped with a magnetic stirrer and reflux condenser was charged with 8 (310 mg, 1.30 mmol), THF (2 mL) and ethanol (2 mL). A solution of lithium hydroxide (125 mg, 5.21 mmol) in water (2 mL) was added, and the mixture was stirred at 50° C. for 2 h. After this time, the organic solvents were removed under reduced pressure, water (6 mL) was added, and the pH was adjusted to 3.0 with 2 N hydrochloric acid. The resulting suspension was filtered and the filter cake washed with water (2 mL). The filter cake was dried to constant weight under vacuum at 40° C. to afford a 100% yield (292 mg) of 9 as a white solid: mp 124-125° C.; 1H NMR (500 MHz, CDCl3) δ 7.93 (s, 1H), 3.10 (s, 2H), 1.34 (5, 6H); MS (ESI+) m/z 211.0 (M+H).

후처리

  1. customA 50-mL single-neck round-bottomed flask equipped with a magnetic stirrer
  2. temperaturereflux condenser
  3. customAfter this time, the organic solvents were removed under reduced pressure, water (6 mL)
  4. additionwas added
  5. filtrationThe resulting suspension was filtered
  6. washthe filter cake washed with water (2 mL)
  7. customThe filter cake was dried to constant weight under vacuum at 40° C.

출처 및 근거

ORD 기록
ord-12a8a035669e4f2cbd5c758c4c700b90
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08598174B2

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