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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175325Generated: November 3, 2026

Ammonium Chloride → HCID 59557719, compound

https://huagongshe.com/reaction/1175325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Trifluoromethoxy)ethyl trifluoromethanesulfonateHCID 10635181—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 59557707HCID 59557707—
SolventAcetonitrileHCID 6342—
ProductHCID 59557719HCID 59557719—

Reaction Steps

To a solution of 2-bromo-5-chloro-4-(4-ethylbenzyl)phenol (AT) (0.12 g, 0.38 mmol) in anhydrous CH3CN (4 mL), was added potassium tert-butoxide [1.0 M solution in tert-butanol] (380 μL, 0.38 mmol) followed by 2-(trifluoromethoxy)ethyl trifluoromethanesulfonate (0.10 g, 0.38 mmol) [prepared as described in the Journal of Organic Chemistry, 2001, 66, 1061-1063]. The reaction mixture was stirred for 15 h at room temperature, after which saturated NH4Cl was added and the mixture was partitioned between EtOAc and brine. The organic layer was dried with anhydrous Na2SO4, filtered and concentrated. The residue was purified by preparative TLC to give intermediate BP (0.06 g, 36%). 1H-NMR (CDCl3, 300 MHz) δ 7.31 (s, 1H), 7.10 (m, 4H), 6.89 (s, 1H), 4.31 (m, 2H), 4.20 (m, 2H), 3.96 (s, 2H), 2.61 (q, J=7.5 Hz, 2H), 1.22 (t, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838498B2
Source datasetuspto-grants-2010_11
ORD IDord-e581e6b0956e480bb6cac81324d85872
Source noteuspto-grants-2010_11