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Dimethylformamide dimethyl acetal → 5-(3-dimethylamino-acryloyl)-3,4-dimethyl-3H-thiazol-2-one

HRID 2113989
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HRID 2113989 반응식
[C:1]([C:4]1[S:8][C:7](=[O:9])[N:6]([CH3:10])[C:5]=1[CH3:11])(=[O:3])[CH3:2].CO[CH:14](OC)[N:15]([CH3:17])[CH3:16]>>[CH3:14][N:15]([CH3:17])[CH:16]=[CH:2][C:1]([C:4]1[S:8][C:7](=[O:9])[N:6]([CH3:10])[C:5]=1[CH3:11])=[O:3]
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참가 물질

3

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HCID 78373Dimethylformamide dimethyl acetalHCID 672693935-acetyl-3,4-dimethyl-3H-thiazol-2-one

생성물 1

HCID 672693735-(3-dimethylamino-acryloyl)-3,4-dimethyl-3H-thiazol-2-one수율 44.5%

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온도
100 °C

실험 절차

5-Acetyl-3,4-dimethyl-3H-thiazol-2-one (4.64 g, 27.10 mmol) and dimethylformamide dimethyl acetal (8.4 mL, 59.62 mmol) were mixed in a dry, argon-flushed flask, and heated at 100° C. for 3 h. The mixture was cooled, producing some precipitation, which was enhanced by the addition of an equal volume of Et2O. The resulting orange solid was filtered and washed with Et2O to give 2.73g of 5-(3-dimethylamino-acryloyl)-3,4-dimethyl-3H-thiazol-2-one. 1H-NMR (d6-DMSO): δ 2.52 (s, 3H), 2.82 (bs, 3H), 3.11 (bs, 3H), 3.22 (s, 3H), 5.10 (d, 1H, J=12.2 Hz), 7.61 (d, 1H, J=11.7 Hz). IR (ATR): 1669 and 1630 cm−1 (CO str).

후처리

  1. customflushed flask
  2. temperatureThe mixture was cooled
  3. customproducing
  4. customsome precipitation, which
  5. additionwas enhanced by the addition of an equal volume of Et2O
  6. filtrationThe resulting orange solid was filtered
  7. washwashed with Et2O

출처 및 근거

ORD 기록
ord-418ea53bdd864cfaaaecf3a4e07793d5
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07432260B2

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