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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409838Generated: October 27, 2026

Tetrabutylammonium Fluoride → (s)-Di-tert-butyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl phosphate

https://huagongshe.com/reaction/409838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(s)-Di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphateHCID 57947500—
SolventTetrahydrofuranHCID 8028—
Product(s)-Di-tert-butyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl phosphateHCID 5794755264.1%

Reaction Steps

To a solution of (S)-di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphate (4.1 g, 7.95 mmol) in THF (40 mL) was added TBAF (1.0 M in THF, 8.0 mL, 8.0 mmol). The resulting solution was stirred at RT for 1 h. The mixture was quenched with sat. NH4Cl and diluted with EtOAc. The organic layer was washed with sat. NH4Cl (×2) and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-di-tert-butyl 4-(3-(2,3-difluorobenzyl)-1-methylureido)-5-hydroxypentyl phosphate (2.52 g, 61%) as a colorless oil. LRMS (M+H+ −2 tBu) m/z 383.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759374B2
Source datasetuspto-grants-2014_06
ORD IDord-afde485676aa4f4481e66cb1f4c629b3
Source noteuspto-grants-2014_06