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Sodium Chloride → HCID 59442652、化合物

HRID 657526
ノート
印刷プレビュー

反応式

HRID 657526 の反応式
[CH:1]([N-]C(C)C)(C)C.[Li+].[Br:9][C:10]1[CH:15]=[C:14]([S:16][CH3:17])[CH:13]=[C:12]([F:18])[CH:11]=1.IC.[Cl-].[Na+]>C1COCC1.C(C1C=CC=CC=1)C>[Br:9][C:10]1[CH:15]=[C:14]([S:16][CH3:17])[CH:13]=[C:12]([F:18])[C:11]=1[CH3:1]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 5234Sodium ChlorideHCID 6328Methyl iodideHCID 2724682Lithium diisopropylamideHCID 534144401-Bromo-3-fluoro-5-(methylsulfanyl)benzene

生成物 1

HCID 59442652HCID 59442652、化合物

試薬・触媒・溶媒 2

HCID 7500Ethylbenzene溶媒
HCID 8028
Tetrahydrofuran
溶媒
3 回

反応条件

温度
-73 °C

実験手順

7.5 ml of a 2 M solution of lithium diisopropylamide in THF/HEP/ethylbenzene (Aldrich) were dissolved in 30 ml of anhydrous THF and cooled to −73° C. A solution of 3.0 g of 1-bromo-3-fluoro-5-methylsulfanylbenzene in 10 ml of anhydrous THF added at a temperature between −73° C. and −67° C. Stirring was continued for 90 min at −75° C., then 1.0 ml of iodomethane was added at this temperature. The mixture was then warmed up to room temperature, 100 ml of a saturated aqueous solution of sodium chloride were added and the mixture was extracted twice with 100 ml each of EA. The extracts were dried and concentrated in vacuo to yield 2.0 g of the title compound as a slight yellow oil that was used without further purification.

後処理

  1. temperatureThe mixture was then warmed up to room temperature
  2. extractionthe mixture was extracted twice with 100 ml each of EA
  3. customThe extracts were dried
  4. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-f9e94107eb79466f96bac6ca262d6c0d
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08076324B2

反応ノート

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