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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171008Generated: November 1, 2026

Tetrabutylammonium Fluoride → HCID 86603462, compound

https://huagongshe.com/reaction/1171008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86603461HCID 86603461—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86603462HCID 866034621,000%

Reaction Steps

To a stirring solution diethyl (3,5-dimethyl-4-triisopropylsilanyloxy-benzenesulfonyl)methylphosphonate in THF (3 mL) at room temperature was added TBAF (0.3 mL, 1 M in THF). It was stirred at room temperature for 2 hrs. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate and water. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with ethyl acetate-hexanes (5:1) to afford diethyl (3,5-dimethyl-4-hydroxybenzenesulfonyl)methylphosphonate as a light yellow oil (70 mg, 1000%): 1H NMR (300 MHz, CDCl3-d6): δ 7.54 (s, 2 H), 4.12 (m, 4 H), 3.65 (d, J=16.8 Hz, 2 H), 2.22 (s, 6 H), 1.22 (d, J=7.2 Hz, 6 H). TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=ethyl acetate-hexanes (5:1); Rf=0.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829552B2
Source datasetuspto-grants-2010_11
ORD IDord-b9fb1df267144c9da1a0401cf041ad61
Source noteuspto-grants-2010_11