Hydroxyamine hydrochloride → HCID 86733921, compound

HRID 1414671Notes

Reaction equation

HRID 1414671 reaction equation
[F:1][CH:2]([F:22])[O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH:10]=[C:9]([CH:14]([CH:19]([F:21])[F:20])[C:15](OC)=[O:16])[CH:8]=[CH:7]2.C[O-].[Na+].Cl.[NH2:27][OH:28]>CO>[F:1][CH:2]([F:22])[O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH:10]=[C:9]([CH:14]([CH:19]([F:21])[F:20])[C:15]([NH:27][OH:28])=[O:16])[CH:8]=[CH:7]2

Participants

5

Procedure

A mixture of 32 g. of methyl 6-difluoromethoxy-2-naphthyl-α-difluoromethylacetate, 10 g. of sodium methoxide, 14 g. of hydroxylamine hydrochloride, and 500 ml. of methanol are allowed to stand for 16 hours. The mixture is then filtered and evaporated. The residue is neutralized by the addition of aqueous 1N hydrochloric acid and extracted by ether. The ether solution is then washed with water, dried, and evaporated to afford 6-difluoromethoxy-2-naphthyl-α-difluoromethyl acethydroxamic acid.

Workup

  1. additionA mixture of 32 g
  2. filtrationThe mixture is then filtered
  3. customevaporated
  4. additionThe residue is neutralized by the addition of aqueous 1N hydrochloric acid
  5. extractionextracted by ether
  6. washThe ether solution is then washed with water
  7. customdried
  8. customevaporated

Sources & evidence

ORD record
ord-9d918f65153440d188cc6f22a717a80f
Source dataset
uspto-grants-1977_01
Patent number
US04001301

Reaction notes

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