HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380670Generated: November 4, 2026
Potassium Hydroxide → HCID 178448926, compound
https://huagongshe.com/reaction/2380670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Tributyltin azide | HCID 4984872 | — |
| Reactant | HCID 53946869 | HCID 53946869 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178448926 | HCID 178448926 | — |
Reaction Steps
A solution of 4.0 g (9.8 mmol) of 3-methoxycarbonyl-3-methyl-butanoic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amide and 4.3 g (13 mmol) of tributyltin azide in 80 ml of o-xylene is reacted analogously to Example 1 for 24 hours. For hydrolysis, the reaction mixture is stirred with 50 ml of 2N potassium hydroxide solution at from 40 bis 50° for 4 hours. The aqueous phase is separated and acidified with 2N hydrochloric acid, and the oil which separates is extracted with ethyl acetate. Washing of the ethyl acetate solution with water, drying over MgSO4 and concentration by evaporation yield 3-carboxy-3-methyl-butanoic acid N-butyl-N-[2'-(1H-tetrazol-5-yl)biphenyl-4-ylmethyl]-amide in the form of a colourless foam that has an Rf value of 0.25 [toluene/isopropanol/glacial acetic acid (170:30:2)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05369110 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-20b063e1b955492d89dc18948eb65658 |
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| Source note | uspto-grants-1994_11 |
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