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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571437Generated: October 31, 2026

Tributyltin Chloride → TRIBUTYL(4-METHOXYPHENYL)STANNANE

https://huagongshe.com/reaction/571437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantHCID 178491912HCID 178491912—
SolventTetrahydrofuranHCID 8028—
ProductTRIBUTYL(4-METHOXYPHENYL)STANNANEHCID 276254780.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To tributyltin chloride (652 mg, 2.00 mmol, 1.00 equiv) in THF (2 mL) at 23° C. was added 4-methoxyphenylmagnesium bromide (0.50 M in THF, 8.0 mL, 4.0 mmol, 2.0 equiv). After stirring for 1.0 hr at 60° C., the reaction mixture was cooled to 0° C. and quenched with saturated aqueous NH4Cl (10 mL), and Et2O (10 mL) was added. The phases were separated and the aqueous phase was extracted with Et2O (2×10 mL). The combined organic phases were washed with brine (10 mL) and dried (Na2SO4). The filtrate was concentrated in vacuo and the residue was purified by fractional distillation to afford 637 mg of the title compound as a colorless oil (80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024093B2
Source datasetuspto-grants-2015_05
ORD IDord-35f2ab8166e645d58d780cb2a677545c
Source noteuspto-grants-2015_05