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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115813Generated: October 28, 2026

Tetramethyltin → HCID 67520306, compound

https://huagongshe.com/reaction/2115813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
ReactantHCID 67520377HCID 67520377—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 67520306HCID 67520306—

Reaction Conditions

Temperature90 °C

Reaction Steps

A resealable tube was charged with methyl 6-hydroxy-4-iodo-1-naphthoate (0.302 g, 0.920 mmol), toluene (5.0 ml), tetramethyltin (0.40 g, 0.30 mL, 2.2 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.042 g, 0.036 mmol). The system was purged with argon and the tube was sealed. The mixture stirred at 90° C. for 24 h and was cooled to RT. The mixture was partitioned between EtOAc and water. The aqueous phase was separated and extracted with EtOAc. The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to afford an orange solid. This material was purified via column chromatography on silica gel (eluting with 0-50% ethyl acetate-hexane) to afford methyl 6-hydroxy-4-methyl-1-naphthoate as an orange brown solid. MS (ESI, pos. ion) m/z: 217.1 (M+H). Mass Calc'd for C13H12O3: 216.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-d525b42ed417480395c6c7d432905504
Source noteuspto-grants-2008_10