HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350912Generated: October 25, 2026
2,6-Dichlorobenzaldehyde → (3-Chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amine
https://huagongshe.com/reaction/1350912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorobenzaldehyde | HCID 6737 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-2-methylbutan-2-amine hydrochloride | HCID 21094547 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amine | HCID 21094546 | 99% |
Reaction Steps
13.3 g (84.0 mmol) of 3-chloro-1,1-dimethyl propylamine-hydrochloride were added to 84.0 mL sodium hydroxide solution (1 M) at 0° C. with vigorous stirring. The reaction mixture was stirred for 30 min at 0° C. and then combined with 50 mL methylene chloride. The phases were separated and the aqueous phase was twice extracted with 35 mL methylene chloride. The combined organic phases were dried over magnesium sulphate and at ambient temperature combined with 14.2 g (81.0 mmol) of 2,6-dichlorobenzaldehyde with stirring. The reaction mixture was stirred for 18 h at ambient temperature, dried again with magnesium sulphate and the solvent was removed. 22.3 g (80.0 mmol, 99%) (3-chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amine were obtained as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214698B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-97b6c5badb5e4b48ab2cce294e41862e |
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| Source note | uspto-grants-2007_05 |
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