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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888314Generated: November 2, 2026

(3-Hydroxy-3-methyloctyl)(triphenyl)phosphonium iodide → ethyl 2-[(2-{(1R,2S,5R)-2-(acetyloxy)-5-[(1E)-4-hydroxy-4-methyl-1-nonenyl]cyclopentyl}ethyl)thio]-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1888314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Hydroxy-3-methyloctyl)(triphenyl)phosphonium iodideHCID 86054281—
ReactantEthyl 2-({2-[(1R,2S,5S)-2-(acetyloxy)-5-formylcyclopentyl]ethyl}thio)-1,3-thiazole-4-carboxylateHCID 86634273—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-[(2-{(1R,2S,5R)-2-(acetyloxy)-5-[(1E)-4-hydroxy-4-methyl-1-nonenyl]cyclopentyl}ethyl)thio]-1,3-thiazole-4-carboxylateHCID 6685830938.1%

Reaction Steps

To a solution of (3-hydroxy-3-methyloctyl)(triphenyl)phosphonium iodide (800 mg) in anhydrous tetrahydrofuran (9.00 mL) was added n-butyllithium (1.60M in hexane, 1.90 mL) at room temperature and the solution was stirred for 1 Hour. To the solution was added a solution of the compound 49 (349 mg) in anhydrous tetrahydrofuran (6.00 mL) was slowly added at −78° C. and the solution was stirred for 2 Hours. The solution temperature was risen to room temperature. The reaction solution was poured into ice water and extracted with ethyl acetate. The organic layer was washed water and brine, dried over anhydrous sodium sulfate and concentrated. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=4:1) to give the title compound (178 mg) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501793B2
Source datasetuspto-grants-2013_08
ORD IDord-3e9d421a4a4b4158ab3cce3b0ae3657a
Source noteuspto-grants-2013_08