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Water → 4-(Hydroxymethyl)-3-methylbenzonitrile

HRID 1250280
ノート
印刷プレビュー

反応式

HRID 1250280 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[CH:10]=C)[C:5]#[N:6].[O:12]=[O+][O-].[BH4-].[Na+].O>CO>[OH:12][CH2:10][C:9]1[CH:8]=[CH:7][C:4]([C:5]#[N:6])=[CH:3][C:2]=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

6

反応物 4

HCID 962WaterHCID 24823OzoneHCID 4311764Sodium borohydrideHCID 183278913-Methyl-4-vinylbenzonitrile

生成物 1

HCID 183278964-(Hydroxymethyl)-3-methylbenzonitrile収率 90%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
-70 °C

実験手順

3-Methyl-4-vinylbenzonitrile (0.40 g; 2.8 mmol; from step (i) above) was dissolved in 50 mL of methanol and cooled to −70° C. Ozone (2 eq.) was bubbled through, and then 0.20 g (5.3 mmol) of sodium borohydride and 5 mL of water were added and the cooling bath was removed. After 4 h the methanol was evaporated and the residue was partitioned between 1M HCl and ether. The aqueous layer was extracted twice with ether and the combined organic phase was washed with water, dried (Na2SO4) and evaporated to yield 0.37 g (90%) of the desired product, which was used in the next step without further purification.

後処理

  1. additionwere added
  2. customthe cooling bath was removed
  3. customAfter 4 h the methanol was evaporated
  4. customthe residue was partitioned between 1M HCl and ether
  5. extractionThe aqueous layer was extracted twice with ether
  6. washthe combined organic phase was washed with water
  7. dry with materialdried (Na2SO4)
  8. customevaporated

出典と根拠

ORDレコード
ord-6aa23f0416354da883ddf147d9477e39
出典データセット
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06337394B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート