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Benzyl Bromide → HCID 11759308、化合物

HRID 1826072
ノート
印刷プレビュー

反応式

HRID 1826072 の反応式
[CH3:1][S:2][CH:3]([C:7]1[CH:12]=[C:11]([CH:13]=[O:14])[CH:10]=[CH:9][C:8]=1[O:15][CH3:16])[C:4]([OH:6])=[O:5].C(=O)([O-])[O-].[K+].[K+].[CH2:23](Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>CN(C)C=O>[CH3:1][S:2][CH:3]([C:7]1[CH:12]=[C:11]([CH:13]=[O:14])[CH:10]=[CH:9][C:8]=1[O:15][CH3:16])[C:4]([O:6][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:5]
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 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 12017994HCID 12017994、化合物

生成物 1

HCID 11759308HCID 11759308、化合物収率 83%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Ethyl 2-methylthio-2-(5-formyl-2-methoxyphenyl)acetate (4.80 g, 17.9 mmol), ethanol (30 mL) and 10% aqueous solution of sodium hydroxide (20 mL) were mixed and the mixture was stirred for 3 hours at room temperature. The reaction mixture was poured in ice water and made acidic with concentrated hydrochloric acid, which was then extracted with ethyl acetate. The extracte was washed with water, dried over anhydrous sodium sulfate, and then concentrated to afford 4.00 g of crude 2-methylthio-2-(5-formyl-2-methoxyphenyl)acetic acid as yellow crystals (this compound was used for next reaction without further purification). Next, 2-methylthio-2-(5-formyl-2-methoxyphenyl)acetic acid (4.00 g, 16.4 mmol) and N,N-dimethylformamide (50 mL) were mixed and, after anhydrous potassium carbonate (3.71 g, 26.8 mmol) and benzyl bromide (3.06 g, 17.9 mmol) were added at room temperature under stirring, the mixture was stirred for 5 hours. The reaction mixture was poured in ice water and extracted with ether. The extracted solution was washed with water and brine, and then dried over anhydrous sodium sulfate. The reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluate n-hexane:ethyl acetate=6:1 v/v) to afford 4.50 g (76%) of the title compound as a light brown oil.

後処理

  1. customwas used for next reaction without further purification)
  2. stirringthe mixture was stirred for 5 hours
  3. extractionextracted with ether
  4. washThe extracted solution was washed with water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationThe reaction mixture was concentrated
  7. customthe residue was purified by silica gel column chromatography (eluate n-hexane:ethyl acetate=6:1 v/v)

出典と根拠

ORDレコード
ord-d796823bfc4f4e9f90625958e7355b5f
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07049342B2

反応ノート

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