HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554098Generated: October 26, 2026
Diisopropylamine → [2-Chloro-3-(trifluoromethyl)phenyl]methyl isocyanide
https://huagongshe.com/reaction/554098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | {[2-Chloro-3-(trifluoromethyl)phenyl]methyl}formamide | HCID 86617531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2-Chloro-3-(trifluoromethyl)phenyl]methyl isocyanide | HCID 86617532 | 106.6% |
Reaction Steps
A solution of {[2-chloro-3-(trifluoromethyl)phenyl]methyl}formamide (0.67 g, 2.82 mmol) in anhydrous dichloromethane (20 ml) was cooled under argon in an ice-water bath before the addition of diisopropylamine (1.78 ml, 12.7 mmol) followed by phosphorus oxychloride (0.393 ml, 4.23 mmol). The reaction was stirred at between 2-5° C. for 2 hrs. The mixture was then reduced in vacuo and the residue treated with saturated aqueous sodium hydrogen carbonate (20 ml) and extracted with dichloromethane (20 ml). The organic layer was passed through a hydrophobic frit and the reduced in vacuo to give a yellow solid. Further drying in vacuo gave [2-chloro-3-(trifluoromethyl)phenyl]methyl isocyanide as an orange gum (0.66 g) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048907B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-8a7f7324880e447caf60995de0fbbff2 |
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| Source note | uspto-grants-2011_11 |
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