HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192308Generated: October 29, 2026
1-Thiophen-2-yl-cyclohept-4-enecarboxylic acid ethyl ester → 1-Thiophen-2-yl-cycloheptanecarboxylic acid ethyl ester
https://huagongshe.com/reaction/2192308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Thiophen-2-yl-cyclohept-4-enecarboxylic acid ethyl ester | HCID 58348331 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Chlorotris(triphenylphosphine)rhodium(I) | HCID 84599 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Thiophen-2-yl-cycloheptanecarboxylic acid ethyl ester | HCID 58348324 | 86.7% |
Reaction Steps
1-Thiophen-2-yl-cyclohept-4-enecarboxylic acid ethyl ester (Example 5b) (2.86 g) was dissolved in ethanol (30 mL) and tris(triphenylphosphine)rhodium(I) chloride (0.100 g) was added. The reaction mixture was stirred rapidly under 5 atmospheres of hydrogen overnight. Further tris(triphenylphosphine)rhodium(I) chloride (0.050 g) was added and the reaction mixture was stirred under 5 atmospheres of hydrogen for 3 days. A third addition of tris(triphenylphosphine)rhodium(I) chloride (0.050 g) was made and the reaction mixture was stirred under 3 atmospheres of hydrogen overnight. The contents were evaporated to dryness and purified on silica eluting with ethyl acetate/isohexane (5/ 95) to afford the sub-titled compound (2.500 g) as a clear almost colourless oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329729B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-6472a42849174177afd228c2e2c320f5 |
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| Source note | uspto-grants-2012_12 |
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