HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052980Generated: October 26, 2026
Chloral alcoholate → N-(4-bromo-2-methoxyphenyl)-2-(hydroxyimino)acetamide
https://huagongshe.com/reaction/1052980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloral alcoholate | HCID 10587 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4-Bromo-2-methoxyaniline | HCID 459257 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-bromo-2-methoxyphenyl)-2-(hydroxyimino)acetamide | HCID 117668132 | 68% |
Reaction Steps
Hydroxylamine hydrochloride (6.67 g, 96 mmol) in water (15 mL) was added to a suspension of 2,2,2-trichloro-1-ethoxyethanol (6.96 g, 36 mmol) and sodium sulfate (38.3 g, 270 mmol) in water (45 mL) and 2N HCl (30 mL). The mixture was stirred at 60° C. for 20 min. 4-Bromo-2-methoxybenzenamine (6.06 g, 30 mol) in 2N HCl (30 mL) was added, and the mixture was heated to 90° C. for 2 h. The mixture was cooled to room temperature. The solid was collected by filtration, washed with water, and air dried to afford the title compound (5.55 g, crude, 68% yield). This material was used in the next step without further purification. MS (ESI) m/e [M+1]+ 273, 275.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09393232B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-93b3f8b4e035460eaa558faf2692cc4c |
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| Source note | uspto-grants-2016_07 |
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