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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500028Generated: November 4, 2026

tert-Butanol → HCID 57818921, compound

https://huagongshe.com/reaction/1500028

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant4-Fluorobenzylic alcoholHCID 68022—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57818481HCID 57818481—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57818921HCID 5781892142%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of (2-chloro-5-fluoropyrimidin-4-yl)-(2-fluorobenzyl)amine* (0.103 g, 0.40 mmol) in 5 mL of dry THF was treated with 4-fluorobenzylalcohol (0.062 g, 0.49 mmol) and a 1.0 M solution of KOtBu in tBuOH (0.4 mL, 0.4 mmol). The mixture was heated at 80° C. in a sealed vial for 18 h, partitioned between CH2Cl2 and water, and the organic phase was washed with brine, dried over Na2SO4, and filtered. The solvent was removed under reduced pressure and the residue purified by flash column chromatography (SiO2, 10→20% EtOAc/petroleum ether) to yield the title compound (0.157 g, 42%) as a white solid: mp 83-84° C.; 1H NMR (300 MHz, CDCl3) δ 7.83 (d, J=2.8, 1H), 7.45-7.27 (m, 5H), 7.15-6.96 (m, 5H), 5.37 (br s, 1H), 5.29 (s, 3H), 4.74 (d, J=5.9, 3H); MS (ESI) m/z 346 (M+H)+. *Singh, R.; Argade, A.; Payan, D. G.; Clough, J.; Keim, H.; Sylvain, C.; Li, H.; Bhamidipati, S., WO 2004014382 A1 20040219

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09204653B2
Source datasetuspto-grants-2015_12
ORD IDord-6fac3538aec9455ab7a729c8577aa8dd
Source noteuspto-grants-2015_12