Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051105Generated: November 4, 2026

Tetrabutylammonium Fluoride → Methyl 2-(3-hydroxyphenoxy)acetate

https://huagongshe.com/reaction/1051105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 2-(3-((t-butyldimethylsilyl)oxy)phenoxy)acetateHCID 125464147—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(3-hydroxyphenoxy)acetateHCID 1026174661.4%

Reaction Steps

Tetrabutylammonium fluoride in THF (1 M, 3.4 mL, 3.4 mmol) was added to a solution of methyl 2-(3-((t-butyldimethylsilyl)oxy)phenoxy)acetate (0.50 g, 1.7 mmol) in THF (5 mL) in a 100 mL round bottom flask. The reaction was allowed to stir overnight at room temperature. The reaction was quenched with saturated aqueous ammonium chloride (100 mL) and extracted with ethyl acetate (200 mL). The organic extract was dried (Na2SO4), filtered and concentrated. The resulting crude residue was purified by combiflash (40 g column, hexanes→100% ethyl acetate/hexanes, gradient) to afford 0.19 g (60%) of methyl 2-(3-hydroxyphenoxy)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388153B2
Source datasetuspto-grants-2016_07
ORD IDord-0510814b9010490fbfb2fe2eb94a51e4
Source noteuspto-grants-2016_07