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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604115Generated: October 31, 2026

Styrene → HCID 15867808, compound

https://huagongshe.com/reaction/1604115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyreneHCID 7501—
ReactantMAGNESIUM SILICATE (synthetic)HCID 61680—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantHCID 15867790HCID 15867790—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15867808HCID 1586780848%

Reaction Steps

Styrene (150 μl, 1.0 mmol) in tetrahydrofuran (3 mL) was ice-cooled, then 9-BBN, (0.5M THF solution, 2.1 mL, 1.05 mmol) was added. This was agitated for 6 hours while gradually raising the reaction temperature to room temperature. Further, to this were added methyl (11R,12S,13E,15S,17R)-9-trifluoromethanesulfonyloxy-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (233 mg, 0.3 mmol), bistriphenylphosphinepalladiumchloride (70 mg, 0.1 mmol), and tripotassium phosphate (255 mg, 1.2 mmol) in tetrahydrofuran (5 mL) suspension. The reaction mixture was agitated at 60° C. for 15 hours. The reaction solution was cooled, then subjected to Florisil column chromotography to remove the metal complexes. The obtained solution was concentrated under reduced pressure, then was purified by silica gel column chromotography (2 to 4% ethyl acetate/hexane) to obtain methyl (11R,12S,13E,15S,17R)-9-phenethyl-11,15-bis(tert-butyldimethylsiloxy)-17,20-dimethyl-7-thiaprosta-8,13-dienoate (104 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990346
Source datasetuspto-grants-1999_11
ORD IDord-c3f4a1565db04b8886bec53476f51e19
Source noteuspto-grants-1999_11