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Acetic Anhydride → HCID 10469565, 화합물

HRID 486080
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HRID 486080 반응식
[OH:1][C:2]1[C:3]([CH3:18])=[C:4]2[C:9](=[C:10]([CH3:13])[C:11]=1[CH3:12])[O:8][C:7]([C:15]([OH:17])=[O:16])([CH3:14])[CH2:6][CH2:5]2.[C:19](OC(=O)C)(=[O:21])[CH3:20]>N1C=CC=CC=1>[C:19]([O:1][C:2]1[C:3]([CH3:18])=[C:4]2[C:9](=[C:10]([CH3:13])[C:11]=1[CH3:12])[O:8][C:7]([C:15]([OH:17])=[O:16])([CH3:14])[CH2:6][CH2:5]2)(=[O:21])[CH3:20]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 40634Trolox

생성물 1

HCID 10469565HCID 10469565, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
30 °C

실험 절차

Dissolve 50 grams (0.2 mol) of (6-hydroxy-2,5,7,8-tetramethylchroman-2-yl)carboxylic acid in 150 cm3 of anhydrous pyridine. Add dropwise 9.4 cm3 (0.1 mol) of acetic anhydride under a stream of nitrogen. Stir for 2 hours at a temperature of 30° C. After cooling, pour the mixture onto some ice, extract the resulting product with diethyl ether, and wash the organic phase with a 0.2N hydrochloric acid solution, and then with water until neutral. After evaporation of the solvent, an oily mass is collected which crystallises after trituration in diisopropyl ether.

후처리

  1. temperatureAfter cooling
  2. additionpour the mixture onto some ice
  3. extractionextract the resulting product with diethyl ether
  4. washwash the organic phase with a 0.2N hydrochloric acid solution
  5. customAfter evaporation of the solvent
  6. customan oily mass is collected which
  7. customcrystallises after trituration in diisopropyl ether

출처 및 근거

ORD 기록
ord-44c8a22aa0794176948a404bb2fc8c93
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05290797

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