HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689796Generated: October 26, 2026
2,6-Dichlorobenzaldehyde → Benzaldehyde, 2,6-dichloro-, oxime
https://huagongshe.com/reaction/1689796
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorobenzaldehyde | HCID 6737 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzaldehyde, 2,6-dichloro-, oxime | HCID 91328 | 99.6% |
Reaction Steps
Sodium hydroxide 3N (3.14 L, 9.43 mol) is added dropwise to a stirred suspension of hydroxylamine hydrochloride (675.55 g, 9.43 mol) in 0.5 L of water at 0° C. To this mixture is added dropwise a suspension of 2,6-dichlorobenzaldehyde (1500 g, 8.57 mol) in 7.5 L of ethanol and the reaction is heated at 90° C. overnight. The mixture is cooled to room temperature and then, concentrated to dryness. The solid is triturated in a mixture of H2O/EtOH, 10:1 (4.4 L), filtered and dried under high vacuum at 45° C. overnight. 1621.78 g of title compound (99% yield) is obtained as a white solid. MS (m/e): 190 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153624B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-c3f0e80f6181496680572301a72f489f |
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| Source note | uspto-grants-2012_04 |
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