HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372Generated: October 27, 2026
Dichloromethane → (1R,2S)-3-oxo-2-pentyl-cyclopentaneacetic acid
https://huagongshe.com/reaction/2372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Oxo-2-pentyl-1 cyclopentene-1-acetic acid | HCID 18421575 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1R,2S)-3-oxo-2-pentyl-cyclopentaneacetic acid | HCID 9920768 | — |
Reaction Steps
Into a Schlenk type vessel, kept anhydrous and under Ar, there was injected the precatalytic solution (6.75 ml) containing 47 mg (0.05 mmole) of bis(trifluoro-acetato)[(+)-(R)-2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl]ruthenium (II), 3-oxo-2-pentyl-1-cyclopentene-1-acetic acid (0.5 g, 2.4 mmole), CH2Cl2 (5 ml), methanol (5 ml) and triethylamine (10.28 mg, 0.1 mmole, 14 μl, dist. over KOH). After stirring for 5 min, the orange soltion was filtered through a single use filter (Acrodisc 0.45 μm) in a dry autoclave (100 ml/107Pa) under Ar. The autoclave was then connected to a source of hydrogen and rinsed 5× with hydrogen at a pressure of 106Pa. The autoclave was then pressurized at 9×106Pa. Stirring at this pressure and 25° was carried out during 120 h. Afterwards, the pressure was gently released, the autoclave opened and the orange solution concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728866 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-a0652456c8c14b52877012b598e65bcc |
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| Source note | uspto-grants-1998_03 |
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