Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774370Generated: November 3, 2026

Diisopropylamine → HCID 13358204, compound

https://huagongshe.com/reaction/1774370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantButanoic acid, 2-bromo-, ethyl esterHCID 79039—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13358204HCID 1335820463%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diisopropylamine (654 mg, 6.46 mmol) in anhydrous tetrahydrofuran (5 mL) under the atmosphere of argon was added a 1.58 M n-butyl lithium-hexane solution (3.9 mL, 6.4 mmol) with stirring under ice cooling, and the mixture was stirred at 0° C. for 10 min and at −90° C. for 5 min. To the mixture, a solution of ethyl 2-bromo-n-butyrate (1.00 g, 5.13 mmol) in anhydrous tetrahydrofuran (9.5 mL) was added dropwise at −90° C., and the mixture was stirred for 30 min. Copper (I) iodide (489 mg, 2.56 mmol) was added at the same temperature, and the mixture was vigorously stirred further 5 min. The temperature was raised to 0° C. with stirring, and a saturated aqueous ammonium chloride solution (30 mL) was added. The reaction mixture was directly filtered, and the filtrate was concentrated under reduced pressure. The residue was diluted with water and extracted twice with ethyl acetate, and the combined organic layer was washed sequentially with water and brine and concentrated. The residue thus obtained was subjected to silica gel column chromatography (hexane-ethyl acetate 9:1) to give 368.4 mg of the title compound as oil (yield: 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260375B2
Source datasetuspto-grants-2016_02
ORD IDord-fac7af51323c4bcc9d754e88726a5b2e
Source noteuspto-grants-2016_02