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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828971Generated: October 26, 2026

Potassium Carbonate → 5-[2-(tert-butoxycarbonyl-ethyl-amino)-propyl]-benzo[1,3]dioxole-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1828971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl dibromoacetateHCID 69237—
Reactant[2-(3,4-Dihydroxy-phenyl)-1-methyl-ethyl]-ethyl-carbamic acid tert-butyl esterHCID 70986816—
SolventDimethylformamideHCID 6228—
Product5-[2-(tert-butoxycarbonyl-ethyl-amino)-propyl]-benzo[1,3]dioxole-2-carboxylic Acid Ethyl EsterHCID 6890000479.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

To 2 g (6.7 mmol) of 2C was added 40 mL of anhydrous DMF followed by 3.5 g (25 mmol) of anhydrous K2CO3, 5 g of 3 A° molecular sieves and 3.2 mL (25 mmol) of ethyl dibromoacetate. The reaction mixture was heated at 120° C. for 3 hours under argon atmosphere and then concentrated under reduced pressure. To the residue 75 mL of ethyl acetate were added and filtered. To the filtrate 75 mL of water were added and transferred to a separatory funnel. The organic layer was separated, and the aqueous layer was extracted with 5×75 mL of ethyl acetate. All the organic layers were combined, dried (anhydrous Na2SO4), and concentrated to dryness. The residue was purified by silica gel column chromatography using 10% ethyl acetate in hexane to give 954 mg (5.3 mmol, 37%) of 2D as a colorless gum (M+Na, 402).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060847B2
Source datasetuspto-grants-2006_06
ORD IDord-7a08d05f0a52457d8c83236575f3f28e
Source noteuspto-grants-2006_06