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Hydrochloric Acid → Methyl (2-hydroxyphenyl)acetate

HRID 129705
ノート
印刷プレビュー

反応式

HRID 129705 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=[O:10].Cl.[CH3:13]O>>[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([O:11][CH3:13])=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 11970(2-Hydroxyphenyl)acetic acid

生成物 1

HCID 89719Methyl (2-hydroxyphenyl)acetate収率 92%

実験手順

2-(Hydroxyphenyl)acetic acid (50 g) was added to a solution of hydrogen chloride in methanol [prepared from acetyl chloride (25 ml) and methanol (250 ml)]. The solution was stirred at room temperature for three hours and then allowed to stand overnight (fifteen hours). The resulting mixture was concentrated under reduced pressure, and the residue was taken up in ether (250 ml) and washed with an aqueous solution of sodium bicarbonate until effervescence ceased. The ethereal solution was dried and then concentrated under reduced pressure and the resulting solid was recrystallized from ether/petrol to afford methyl (2-hydroxyphenyl)acetate (50 g; 92% yield) as white, powdery crystals, top. 70°-72° C.; infrared max. (nujol mull): 3420, 1715 cm-1 ; 1H nmr (90 MHz): delta 3.70 (2H,s), 3.75 (3H,s), 6.80-6.95 (2H,m), 7.05-7.10 (1H,m), 7.15-7.25 (1H,m), 7.40 (1H, s) ppm.

後処理

  1. waitto stand overnight
  2. custom(fifteen hours)
  3. concentrationThe resulting mixture was concentrated under reduced pressure
  4. washwashed with an aqueous solution of sodium bicarbonate until effervescence
  5. customThe ethereal solution was dried
  6. concentrationconcentrated under reduced pressure
  7. customthe resulting solid was recrystallized from ether/petrol

出典と根拠

ORDレコード
ord-ddcf66038df241f09c6266db14ccbd6a
出典データセット
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05470819

反応ノート

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