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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197565Generated: October 31, 2026

Tributyltin Chloride → HCID 58207969, compound

https://huagongshe.com/reaction/2197565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 58207984HCID 58207984—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58207969HCID 5820796940.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

LDA (0.55M 1.1 mmol, 2M) was added to a RBF containing THF (5 mL) cooled to −78° C. A solution of tert-butyl isopropyl(thiazol-2-yl)carbamate (242 mg, 1 mmol) in THF (5 mL) was added via cannula and the resulting solution stirred for 2 h at −78° C. Tributyltin chloride (0.27 mL, 1 mmol) was added and the reaction mixture allowed to slowly warm to room temperature then stirred overnight. The reaction mixture was then quenched with NH4Cl (2 mL, sat. aq.) and diluted with water. The mixture was then extracted with EtOAc (3×25 mL) and the combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo. The product was isolated via column chromatography (SiO2, 2% EtOAc/heptane) to afford the product (214 mg, 40% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338604B2
Source datasetuspto-grants-2012_12
ORD IDord-6eabc2831afa4512abae137fc07d6d33
Source noteuspto-grants-2012_12