Hydroxyamine hydrochloride → HCID 86733921, compound

HRID 840039Notes

Reaction equation

HRID 840039 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-2481a993f1434ec5852ca7f1ecb615a9
Source dataset
uspto-grants-1978_06
Patent number
US04097674

Reaction notes

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