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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Hydroxy-3-methyloctyl)(triphenyl)phosphonium iodide | HCID 86054281 | — |
| Reactant | Ethyl 2-({2-[(1R,2S,5S)-2-(acetyloxy)-5-formylcyclopentyl]ethyl}thio)-1,3-thiazole-4-carboxylate | HCID 86634273 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 2-[(2-{(1R,2S,5R)-2-(acetyloxy)-5-[(1E)-4-hydroxy-4-methyl-1-nonenyl]cyclopentyl}ethyl)thio]-1,3-thiazole-4-carboxylate | HCID 66858309 | 38.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501793B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-3e9d421a4a4b4158ab3cce3b0ae3657a |
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| Source note | uspto-grants-2013_08 |
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