HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846511Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 19882813, compound
https://huagongshe.com/reaction/846511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | HCID 19882809 | HCID 19882809 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19882813 | HCID 19882813 | 20.7% |
Reaction Steps
To a stirred solution of 0.5 g (0.0017 mole) of 1-(2,4-dichloro-5-hydroxyphenyl)-1,4-dihydro-4-propyl-5H-tetrazol-5-one (Example 10, Step A) and 0.15 g (0.0021 mole) of 2-butyn-1-ol in 5 mL of acetonitrile was added 0.33 g (0.0016 mole) of dicyclohexylcarbodiimide. The reaction mixture was heated at reflux temperature for 4 days, cooled to room temperature, and filtered. The filtrate was washed with 10 mL of a 10% aqueous sodium hydroxide solution, diluted with methylene chloride, and washed with 10 mL of 6N hydrochloric acid. The washed organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate evaporated to leave an oil. The oil was purified by column chromatography on silica gel, eluting with ethyl acetate: heptane (20:80), to yield 0.12 g of 1-[2,4-dichloro-5-(2-butynyloxy)phenyl]-1,4-dihydro-4-propyl-5H-tetrazol-5-one as a solid, mp 58°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05136868 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-f1aec66fef634e2e88c8e4b96bd86973 |
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| Source note | uspto-grants-1992_08 |
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