HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409627Generated: October 31, 2026
Diisopropylamine → HCID 53386304, compound
https://huagongshe.com/reaction/409627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | HCID 53386303 | HCID 53386303 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53386304 | HCID 53386304 | 88.3% |
Reaction Steps
1000 mL THF and 132.27 g diisopropyl amine were taken in round bottom flask at 25° C. The reaction mixture was cooled to −10° C. and 531 mL of n-butyl amine was added to it. The reaction mixture was stirred for 30 minutes and further cooled to −40° C. 113 g N,N-dimethylacetamide solution in 1000 mL THF was gradually added to the reaction mixture and stirred for 2 hours. 100 g (S)-Ethyl-3-hydroxy-4-(1-phenyl-1H-tetrazol-5-ylthio)butanoate (11a) solution in 200 mL THF was added to the reaction mixture and stirred for 2 hours. After the completion of the reaction as monitored by TLC, the reaction mixture was quenched with 20% 1000 mL ammonium chloride solution at about −25° C. The separated aqueous layer was extracted with 400 mL ethyl acetate. The separated organic layer was washed with 1000 mL 1N HCl solution followed by washing with 1000 mL of water at 25° C. The organic layer was distilled under vacuum below 50° C. to obtain 100 g residue as an oil. The oily residue was taken in 400 mL hexane and distilled to obtain oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759518B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-6c3fd229872a47b8865db8eb589ab580 |
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| Source note | uspto-grants-2014_06 |
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