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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244484Generated: October 30, 2026

Tin tetrachloride → HCID 86584206, compound

https://huagongshe.com/reaction/1244484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTin tetrachlorideHCID 24287—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86600355HCID 86600355—
SolventEthyl AcetateHCID 8857—
ProductHCID 86584206HCID 8658420653%

Reaction Conditions

Temperature70 °C

Reaction Steps

In a 100 ml flask equipped with a refrigerant, 0.9 g (2.18 mmoles) of 3-[(3,5-bis-(1,1-dimethylethyl)-4-hydroxyphenyl]-N-(4-hydroxy-3-nitrophenyl)-2-propenamide is dissolved in 20 ml of ethyl acetate, 2.46 g (10.9 mmoles) of tin chloride (dihydrate) is added and the mixture is heated at 70° C. for three hours. After returning to ambient temperature, the reaction medium is poured onto an agitated solution of sodium bicarbonate (0.1 M), a precipitate forms, which is eliminated by filtration on celite. The filtrate is decanted and the aqueous phase is extracted with 20 ml of ethyl acetate. The organic phases are collected together and washed with 20 ml of water followed by 20 ml of a saturated solution of sodium chloride. After drying over sodium sulphate and filtration, the organic solution is concentrated to dryness, under partial vacuum. The evaporation residue is suspended in a heptane/ethyl acetate mixture (1/1) and filtered to produce a yellowish powder with a yield of 53%. The product is used as it is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122535B2
Source datasetuspto-grants-2006_10
ORD IDord-fc9643e0179d439bbda3b68ec4b625dc
Source noteuspto-grants-2006_10