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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757212Generated: November 2, 2026

Potassium hydroxy sulfite → HCID 19425522, compound

https://huagongshe.com/reaction/1757212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydroxy sulfiteHCID 23707502—
ReactantHCID 131719101HCID 131719101—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 19425522HCID 19425522—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of methyl (E)-6-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate (10.6 g) in methylene chloride (150 ml), methanol (150 ml) and pyridine (5 ml) was treated with an excess of Oxone® at -70° C. The reaction was quenched with dimethylsulfide (20 ml) and stirred for 5 hours at 25° C. The reaction mixture was poured into 1N aqueous sodium hydrogen sulfate. Extraction with 1:1 ethyl acetate:hexane gave an oil which on purification by silica gel chromatography gave 2-(4-t-butyldimethylsilyloxy-1,3-dihydro-6-ethyl-7-methyl-3-oxoisobenzofuran-5-yl)-acetaldehyde, m.p. 90.9°-91.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444072
Source datasetuspto-grants-1995_08
ORD IDord-fb943852ef2340918499b68dc17b191f
Source noteuspto-grants-1995_08