Sodium Hydroxide → 3-Bromo-thiophene-2-carbaldehyde oxime

HRID 456533Notes

Reaction equation

HRID 456533 reaction equation
[Br:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[CH:7]=O.Cl.[NH2:10][OH:11].[OH-].[Na+]>C(O)C.O>[Br:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[CH:7]=[N:10][OH:11]

Participants

6

Conditions

Temperature
0 °C

Procedure

3-Bromothiophene-2-carbaldehyde (Maybridge) (28.7 gm, 0.15 mol) in ethanol (50 ml) was added in one portion to a solution of hydroxylamine hydrochloride (13.8 gm, 0.2 mole), sodium hydroxide (8 gm, 0.2 mol) in water (30 ml) and ethanol (100 ml). The mixture was stirred at 0° C. for 2 hours and was kept at 0° C. overnight. The reaction mixture was diluted with cold water (600 ml), and the precipitated solids were collected by filtration to provide 20.5 gm, (67%) of product. The aqueous layer was further extracted with ethyl acetate and, the combined organic layers were washed with brine, dried with magnesium sulfate filtered and concentrated in vacuo to leave an additional 6.9 g of product.

Workup

  1. waitwas kept at 0° C. overnight
  2. filtrationthe precipitated solids were collected by filtration

Sources & evidence

ORD record
ord-e5cdf39aa3074c89b45086866986166a
Source dataset
uspto-grants-2007_03
Patent number
US07186724B2

Reaction notes

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