HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422539Generated: October 26, 2026
Ethyl chloroformate → [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine
https://huagongshe.com/reaction/422539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine | HCID 49866033 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine | HCID 44511399 | 80% |
Reaction Steps
To a solution of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine (2 mmol) in chloroform was added ethylchloroformate (>10 equiv.) and NaHCO3 (>20 equiv.) and this solution was refluxed for 3 h. After that, chloroform was evaporated and ethyl acetate was added and then this organic layer was washed with water 3 times. It was dried over MgSO4, filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was dissolved in ethanol and potassium hydroxide (>20 equiv.) dissolved in water was added and refluxed for 3 days. After that, ethyl acetate and sat. NaHCO3 were added and the organic layer was extracted. It was dried over MgSO4, filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate and methanol: Yield 80%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101642B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c418652902ec4662b5ea49a0f7fa91a6 |
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| Source note | uspto-grants-2012_01 |
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