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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513102Generated: November 4, 2026

Tributylphosphine → HCID 57791929, compound

https://huagongshe.com/reaction/1513102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantEthyl (4-mercapto-2-methylphenoxy)acetateHCID 16641178—
Reactant(3-Bromo-5-{[tert-butyl(dimethyl)silyl]oxy}phenyl)methanolHCID 57791917—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 57791929HCID 57791929—

Reaction Steps

[3-Bromo-5-(tert-butyl-dimethyl-silanyloxy)-phenyl]-methanol (6.4 g; 20.17 mmol) and (4-mercapto-2-methyl-phenoxy)-acetic acid ethyl ester (5.02 g; 22.19 mmol) were dissolved in THF (200 mL). Tributylphosphine (8.15 g; 40.34 mmol) and 1,1′-(azodicarbonyl)dipiperidine (10.17 g; 40.34 mmol) were added, and the reaction mixture was stirred for 14 h at room temperature. Water and ethyl acetate were added to the reaction mixture. The phases were separated. The organic phase was washed with water, dried, and evaporated. The crude product was purified by flash chromatography (heptane: dichloromethane (1:1)). Yield: 8 g; 80%. HPLC-MS: m/z: 527.0 (M+1); Rt: 3.10 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217086B2
Source datasetuspto-grants-2012_07
ORD IDord-15bcc24882b54a22b63a3d14d78e607f
Source noteuspto-grants-2012_07