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Hydrochloric Acid → 2-Hydroxy-4-methylbenzaldehyde

HRID 22928
ノート
印刷プレビュー

反応式

HRID 22928 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.Cl[Sn](Cl)(Cl)Cl.[CH2:14]=[O:15].Cl>C1(C)C=CC=CC=1.O>[OH:8][C:4]1[CH:3]=[C:2]([CH3:1])[CH:7]=[CH:6][C:5]=1[CH:14]=[O:15]
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 313Hydrochloric AcidHCID 342M-CresolHCID 712FormaldehydeHCID 24287Tin tetrachloride

生成物 1

HCID 612002-Hydroxy-4-methylbenzaldehyde収率 25.5%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 1140
Toluene
溶媒

反応条件

温度
100 °C

実験手順

To a stirred solution of 3-methyl-phenol (1 g, 9.2 mmol) in toluene (5 ml) at room temperature under nitrogen was added SnCl4 (241 mg, 0.92 mmol) and tri-nbutylamine (0.6 ml, 2.77 mmol). After 20 min, paraformaldehyde (611 mg, 20.3 mmol) was added and the whole stirred at 100° C. for 16 h. The reaction mixture was diluted with water (20 ml) and acidified with 2N HCl to pH2. The solution was extracted with ether (25 ml), washed with brine (20 ml), dried (MgSO4) filtered and evaporated to a brown oil. This oil was purified by column chromatography using 5% EtOAc in pentane as eluant to provide the title product (319 mg, 25%); 1HNMR (400 MHz, CDCl3) δ: 2.3 (s, 3H), 6.75 (m, 2H), 7.35 (d, 1H), 9.75 (s, 1H), 11.00 (s, 1H).

後処理

  1. extractionThe solution was extracted with ether (25 ml)
  2. washwashed with brine (20 ml)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customevaporated to a brown oil
  6. customThis oil was purified by column chromatography

出典と根拠

ORDレコード
ord-967ddfe73b30491d9915c6116112b85f
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06849649B2

反応ノート

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