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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409627Generated: October 31, 2026

Diisopropylamine → HCID 53386304, compound

https://huagongshe.com/reaction/409627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantButylamineHCID 8007—
ReactantDimethylacetamideHCID 31374—
ReactantHCID 53386303HCID 53386303—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53386304HCID 5338630488.3%

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759518B2
Source datasetuspto-grants-2014_06
ORD IDord-6c3fd229872a47b8865db8eb589ab580
Source noteuspto-grants-2014_06