Hydrochloric Acid → HCID 131711552, compound

HRID 971442Notes

Reaction equation

HRID 971442 reaction equation
Cl[CH:2](Cl)[C:3]([C:5]1[CH:6]=[CH:7][C:8]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:9]([CH:14]=1)[C:10]([O:12][CH3:13])=[O:11])=[O:4].[Na].Cl.C[OH:27]>>[OH2:4].[O:27]=[CH:2][C:3]([C:5]1[CH:6]=[CH:7][C:8]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:9]([CH:14]=1)[C:10]([O:12][CH3:13])=[O:11])=[O:4]

Participants

5

Reactant 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 5360545SodiumHCID 71372733Methyl 2-(benzyloxy)-5-(dichloroacetyl)benzoate

Product 1

HCID 131711552HCID 131711552, compound

Procedure

5-(Dichloroacetyl)-2-(phenylmethoxy)benzoic acid, methyl ester (2.4 g) was added to sodium (0.34 g) in dry methanol (80 ml). The solution was boiled for 20 min. 0.1 N Hydrochloric acid (40 ml) was added and the solution was boiled for 30 min. The methanol was evaporated off and the mixture was extracted with ether (3×50 ml). The extracts were dried (MgSO4) and evaporated to leave crude 5-(oxoacetyl)-2-(phenylmethoxy)benzoic acid, methyl ester, hydrate as a gum.

Workup

  1. waitthe solution was boiled for 30 min
  2. customThe methanol was evaporated off
  3. extractionthe mixture was extracted with ether (3×50 ml)
  4. dry with materialThe extracts were dried (MgSO4)
  5. customevaporated

Sources & evidence

ORD record
ord-46dc6b95a600433e9044b52b15e24bca
Source dataset
uspto-grants-1979_07
Patent number
US04160036

Reaction notes

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