Hydrochloric Acid → Methyl (2-hydroxyphenyl)acetate

HRID 129705

Reaction equation

HRID 129705 reaction equation
[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]

Participants

4

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-ddcf66038df241f09c6266db14ccbd6a
Source dataset
uspto-grants-1995_11
Patent number
US05470819

Linked notes

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