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Acetic Anhydride → 4-Tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole

HRID 487678
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HRID 487678 반응식
[C:1]([C:5]1[N:6]=[C:7]([CH2:10][O:11][C:12]2[CH:17]=[CH:16][C:15]([CH:18]=[O:19])=[CH:14][C:13]=2[CH:20]=O)[S:8][CH:9]=1)([CH3:4])([CH3:3])[CH3:2].C(OC(=O)C)(=O)C>C1(C)C(C)=CC=CC=1>[C:1]([C:5]1[N:6]=[C:7]([C:10]2[O:11][C:12]3[CH:17]=[CH:16][C:15]([CH:18]=[O:19])=[CH:14][C:13]=3[CH:20]=2)[S:8][CH:9]=1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 190927824-Tert-butyl-2-(2,4-diformylphenoxymethyl)thiazole

생성물 1

HCID 196038064-Tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole수율 1,232.1%

시약·촉매·용매 1

HCID 7237O-Xylene용매

반응 조건

온도
130 °C

실험 절차

A mixture of 4-tert-butyl-2-(2,4-diformylphenoxymethyl)thiazole (0.95 g) and acetic anhydride (12.9 ml) in dried xylene (100 ml) was stirred at 130° C. for 27 hours. After being cooled, the resulting mixture was concentrated in reduced pressure to give a residue. The residue was crystallized with diisopropyl ether. The resulting crystals were collected by filtration and washed with diisopropyl ether to give 4-tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole (11.01 g).

후처리

  1. temperatureAfter being cooled
  2. concentrationthe resulting mixture was concentrated in reduced pressure
  3. customto give a residue
  4. customThe residue was crystallized with diisopropyl ether
  5. filtrationThe resulting crystals were collected by filtration
  6. washwashed with diisopropyl ether

출처 및 근거

ORD 기록
ord-b438139a8fce408ebc4524e60f554a70
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05296495

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