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Triethylamine → HCID 11637840、化合物

HRID 853171
ノート
印刷プレビュー

反応式

HRID 853171 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:15]=[CH:16][CH:17]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][OH:14])=[CH:9][CH:8]=1.C(N(CC)CC)C.[CH3:25][N:26]=[C:27]=[O:28]>ClCCl>[F:1][C:2]1[CH:3]=[C:4]([CH:15]=[CH:16][CH:17]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][O:14][C:27](=[O:28])[NH:26][CH3:25])=[CH:9][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 12228Methyl IsocyanateHCID 887902(4-((3-Fluorophenyl)methoxy)phenyl)methanol

生成物 1

HCID 11637840HCID 11637840、化合物収率 47%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

In a sealed glass tube, a solution of 1.0 g of [4-(3-fluoro-benzyloxy)-phenyl]-methanol [Example 25b)], 0.03 ml of triethylamine and 0.245 g of methyl isocyanate in 40 ml of dichloromethane was heated at 40° C. for 3 d. At that time a transformation rate of 50% was reached, determined by NMR. For the working-up, the reaction mixture was cooled and evaporated. The residue was dissolved in 2 ml of pyridine and 1 ml of acetic acid anhydride and the solution stirred at room temperature for 3 h. Thereafter, the mixture was evaporated under reduced pressure. For purification, the crude material obtained was chromatographed on silica gel using a 2:1-mixture of heptane and ethyl acetate as the eluent. There were obtained 580 mg (47% of theory) of methyl-carbamic acid 4-(3-fluoro-benzyloxy)-benzyl ester as a white solid; MS: m/e=289 (M)+.

後処理

  1. temperaturethe reaction mixture was cooled
  2. customevaporated
  3. dissolutionThe residue was dissolved in 2 ml of pyridine
  4. customThereafter, the mixture was evaporated under reduced pressure
  5. customFor purification
  6. customthe crude material obtained
  7. customwas chromatographed on silica gel using a 2

出典と根拠

ORDレコード
ord-6725ba31080843df94a4de13932c315f
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07253318B2

反応ノート

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