Hydroxylamine → HCID 85086496, compound

HRID 2245772Notes

Reaction equation

HRID 2245772 reaction equation
C[O:2][C:3](=O)[CH:4]=[CH:5][CH:6]=[CH:7][CH2:8][S:9][C:10]1[CH:19]=[CH:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=1.[NH2:21][OH:22].[OH-].[K+].CO>C1COCC1>[OH:22][NH:21][C:3](=[O:2])[CH:4]=[CH:5][CH:6]=[CH:7][CH2:8][S:9][C:10]1[CH:19]=[CH:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

To a solution of 6-(naphthalen-2-ylsulfanyl)-hexa-2,4-dienoic acid methyl ester (0.505 g, 1.78 mmol) in distilled THF (10 mL) containing 50% aqueous hydroxylamine (1.08 mL, 16.4 mmol) was added at 0° C. a solution of potassium hydroxide in methanol (1M, 2.5 ml, 2.5 mmol) over a period of 30 minutes. After stirring the mixture at 0° C. for an additional hour, distilled water (10 mL) was added and the mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C. The solution was extracted with ethyl acetate (2×50 mL), and the combined extracts were dried over anhydrous MgSO4, and evaporated to dryness. The solid residue was recrystallised from ethyl acetate to give the title compound (0.315 g, 62%) as a white solid.

Workup

  1. distillationdistilled water (10 mL)
  2. additionwas added
  3. additionthe mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C
  4. extractionThe solution was extracted with ethyl acetate (2×50 mL)
  5. dry with materialthe combined extracts were dried over anhydrous MgSO4
  6. customevaporated to dryness
  7. customThe solid residue was recrystallised from ethyl acetate

Sources & evidence

ORD record
ord-fce186ff40064af69e73f36c58e0e44a
Source dataset
uspto-grants-2010_03
Patent number
US07683185B2

Reaction notes

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