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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099713Generated: October 30, 2026

Lithium → [2-(2-Aminomethyl-benzo[1,3]dioxol-5-yl)-1-methyl-ethyl]-ethyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2099713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithiumHCID 3028194—
Reactant[2-(2-carbamoyl-benzo[1,3]dioxol-5-yl)-1-methyl-ethyl]-ethyl-carbamic Acid Tert-Butyl EsterHCID 68896083—
SolventTetrahydrofuranHCID 8028—
Product[2-(2-Aminomethyl-benzo[1,3]dioxol-5-yl)-1-methyl-ethyl]-ethyl-carbamic acid tert-butyl esterHCID 7098664175.2%

Reaction Conditions

Temperature-60 °C

Reaction Steps

A flask containing 20 mL of freshly distilled THF was cooled to −60° C., and 615 mg (16.2 mmol) of lithium aluminun hydride (LAH) was added To the reaction mixture, a solution of 1.8 g (5.13 mmol) 2E in 20 mL of freshly distilled THF was added dropwise under argon atmosphere. The reaction mixture was allowed to stir at −60° C. for 20 minutes, 45 minutes at 0° C. and 2 hours at room temperature. The reaction was quenched with 430 μL of 15% NaOH and 3 mL of water and allowed to stir at room temperature for 10 minutes. The resulting solution was filtered through CELITE and the residue was washed with 100 mL of THF. The filtrate was concentrated to dryness under reduced pressure and purified by silica gel column chromatography using ethyl acetate as eluent to give 1.3 g (3.86 mmol, 75%) of 2F as a colorless gum (M+Na, 359).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569676B2
Source datasetuspto-grants-2009_08
ORD IDord-10aff710464946528f2789f4bc8150c1
Source noteuspto-grants-2009_08