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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604108Generated: November 2, 2026

Hexane → HCID 15867797, compound

https://huagongshe.com/reaction/1604108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 15867790HCID 15867790—
ReactantTrimethylaluminumHCID 16682925—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DichloroethaneHCID 11—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
ProductHCID 15867797HCID 1586779755.1%

Reaction Steps

To tetrakistriphenylphosphinepalladium prepared in advance in the system from tris(dibenzylideneacetone) dipalladium(0) (92 mg, 0.1 mmol) and triphenylphosphine (210 mg, 0.8 mmol) were added methyl (11R,12S,13E,15S,17R)-9-trifluoromethanesulfonyloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate 437 mg, 0.546 mmol) in 1,2-dichloroethane (5 mL) and 2M trimethylaluminum in hexane (0.423 mL, 0.846 mmol). This was agitated for 3 hours at room temperature. Ether was added to dilute the reaction solution, then the solution was poured in 1N hydrochloric acid. The desired product was extracted with ether from the mixture. The extract was washed with brine, then was dried over anhydrous sodium sulfate. The solution was concentrated under reduced pressure, then was purified by silica gel column chromotography (2% ethyl acetate/hexane) to obtain methyl (11R,12S,13E,15S,17R)-9-methyl-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (193 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990346
Source datasetuspto-grants-1999_11
ORD IDord-d87e7d7b2e5b4dd8a3fb070ba85f22f5
Source noteuspto-grants-1999_11