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Water → HCID 13071286、化合物

HRID 905087
ノート
印刷プレビュー

反応式

HRID 905087 の反応式
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[H-].[Na+].S(O[CH2:25][CH:26]1[CH2:31][CH2:30][CH:29]=[CH:28][O:27]1)(C1C=CC(C)=CC=1)(=O)=O.O>CN(C)C=O>[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:25][CH:26]2[CH2:31][CH2:30][CH:29]=[CH:28][O:27]2)=[CH:7][CH:6]=1)(=[O:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1983AcetaminophenHCID 24758Sodium hydrideHCID 13071283(3,4-dihydro-2H-pyran-2-yl)methyl 4-methylbenzene-1-sulfonate

生成物 1

HCID 13071286HCID 13071286、化合物収率 78.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of 831 mg of 4-acetamidophenol in 5 ml of dimethylformamide was stirred for 30 minutes at room temperature with 240 mg of 55% sodium hydride. 1.34 g of 2-tosyloxymethyl-3,4-dihydro-2H-pyran was then added and the mixture was heated, with stirring, at 90°-95° C. for 4.5 hours. The mixture was then poured into water and extracted with diethyl ether. The ethereal extract was washed with water and dried over anhydrous magnesium sulphate, after which the solvent was evaporated off. The residue was purified by column chromatography through silica gel, to give 965 mg of the title compound, melting at 114°-116° C.

後処理

  1. temperaturethe mixture was heated
  2. extractionextracted with diethyl ether
  3. extractionThe ethereal extract
  4. washwas washed with water
  5. dry with materialdried over anhydrous magnesium sulphate
  6. customafter which the solvent was evaporated off
  7. customThe residue was purified by column chromatography through silica gel

出典と根拠

ORDレコード
ord-34eb2385b3164b2e9dc261204050e757
出典データセット
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04421758

反応ノート

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