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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220174Generated: October 28, 2026

N,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2) → HCID 59238323, compound

https://huagongshe.com/reaction/220174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N-Tributylbutan-1-aminium fluoride--hydrogen fluoride (1/1/2)HCID 11748636—
Reactant(E)-[2-(3-{4-[1-(4-Bromo-phenylcarbamoyl)-3-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenyl}-acryloylamino)-phenyl]-carbamic acid tert-butyl esterHCID 59238282—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59238323HCID 59238323—

Reaction Steps

To a solution of (E)-[2-(3-{4-[1-(4-bromo-phenylcarbamoyl)-3-(tert-butyl-dimethyl-silanyloxy)-propyl]-phenyl}-acryloylamino)-phenyl]-carbamic acid tert-butyl ester (1.6 g, 2.26 mmol) in THF (40 mL) was added tetrabutylammonium dihydrogen trifluoride (1.36 g, 4.52 mmol). This mixture was stirred at room temperature overnight and then evaporated to remove THF. The mixture was dissolved in water and extracted with ethyl acetate (3×30 mL). The combined organic layer was washed with brine, dried with Na2SO4, filtered, and evaporated. The crude product was purified by column chromatography (CH2Cl2:EtOAc=10:1) to get yellow solid product. MS: calc'd 594 (MH+), exp 594 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202866B2
Source datasetuspto-grants-2012_06
ORD IDord-b32e868c6d2b43aea803d8f3db5e32f9
Source noteuspto-grants-2012_06