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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Thiophen-2-yl-cyclohept-4-enecarboxylic acid ethyl esterHCID 58348331—
ReactantHCID 178418361HCID 178418361—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventEthanolHCID 702—
Product1-Thiophen-2-yl-cycloheptanecarboxylic acid ethyl esterHCID 5834832486.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-6472a42849174177afd228c2e2c320f5
Source noteuspto-grants-2012_12