HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462056Generated: October 26, 2026
Dimethylformamide → N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochloride
https://huagongshe.com/reaction/462056
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,2-Trichloroethanimidamide | HCID 35608 | — |
| Reactant | 2-Acetoxy-3-phenoxy-propylamine hydrochloride | HCID 12504701 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochloride | HCID 178476389 | — |
Reaction Steps
Triethylamine (0.50 g., 5.0 mmoles) is added in small portions over 10 minutes to a well stirred mixture of 1.23 g. (5.0 mmoles) of 2-acetoxy-3-phenoxy-propylamine hydrochloride and 1.61 g. (10 mmoles) of trichloroacetamidine in 5 ml. of dimethylformamide. The reaction mixture is heated at 60° C. for 2 hours, diluted with water and extracted with benzene. The benzene extract is washed with water, dried over magnesium sulfate, filtered and concentrated. The residue is dissolved in benzene and treated with an excess of ethanolic hydrogen chloride. Concentration to dryness affords N-(2-acetoxy-3-phenoxypropyl) trichloroacetamidine hydrochloride with a m.p. of 70° to 77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04065465 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-04ec3107b7904c1f8865f7ad8b66703f |
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| Source note | uspto-grants-1977_12 |
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