Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106601Generated: October 30, 2026

Diisopropylamine → HCID 22880251, compound

https://huagongshe.com/reaction/1106601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1,1-Trifluoro-2-iodoethaneHCID 67709—
ReactantLithiumHCID 3028194—
Reactant81037-06-1HCID 9920448—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22880251HCID 2288025138.2%

Reaction Conditions

Temperature-45 °C

Reaction Steps

To a solution of lithium diiospropylamide (prepared from 13 ml of diisopropylamine and 54 ml of 1.6 M n-BuLi in hexanes in 200 ml of anhydrous THF at 0° C.) at -72° C. was added slowly 2-(s)-t-butyl-5-(s)-methyl-1,3-dioxolan-4-one (12.95 g, 81.9 mmol, Tetrahedron, 1984, 40, 1313) at such a rate as to maintain the internal temperature below -60° C. and the mixture was aged at -72° C. for an hour. 1,1,1-Trifluoro-2-iodoethane (25 g, 119 mmol) was added quickly, the reaction temperature increased to -45° C. and the mixture was aged at -72° C. for 45 min. and then allowed to warm up to -20° C. over 20 min. Saturated aq. NH4Cl was then added and the product was extracted in i-PrOAc, dried over Na2SO4, concentrated and distilled under reduced pressure to afford 7.51 g of a brown oil BP 90° C./20 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057319
Source datasetuspto-grants-2000_05
ORD IDord-1964c3366ec941b082068116465e80d0
Source noteuspto-grants-2000_05