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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429383Generated: November 3, 2026

(R)-tert-Butyl(1-((2-(bromomethyl)benzyl)oxy)pent-4-en-2-yl)carbamate → (R)-1((2-(Bromomethyl)benzyl)oxy)pent-4-en-2-amine

https://huagongshe.com/reaction/1429383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-tert-Butyl(1-((2-(bromomethyl)benzyl)oxy)pent-4-en-2-yl)carbamateHCID 68233279—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product(R)-1((2-(Bromomethyl)benzyl)oxy)pent-4-en-2-amineHCID 6823327798%

Reaction Steps

A solution of compound 18j (2.8 g, 7.3 mmol) in TFA/DCM (25 mL, v/v=1/4) was stirred at rt for 1 hr. The mixture was concentrated under reduced pressure to give compound 18k (2.0 g, 98% yield), which was used without purification. LCMS (m/z): 285.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940722B2
Source datasetuspto-grants-2015_01
ORD IDord-e1d3db3e29cd4390b6c6110979fd38dc
Source noteuspto-grants-2015_01