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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549541Generated: October 30, 2026

Tributylphosphine → HCID 57791929, compound

https://huagongshe.com/reaction/549541

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 numberUS07943669B2
Source datasetuspto-grants-2011_05
ORD IDord-b6959a4cbd524277a2ff2c0ba05f0ce9
Source noteuspto-grants-2011_05