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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400315Generated: November 2, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 57661613, compound

https://huagongshe.com/reaction/2400315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant12-Oxo-dodecanoic acid methyl esterHCID 10421317—
ReactantHCID 69028200HCID 69028200—
ReactantHCID 86629717HCID 86629717—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 57661613HCID 57661613—

Reaction Conditions

Temperature80 °C

Reaction Steps

12-Oxo-dodecanoic acid methyl ester (14.5 g, 63.4 mmol) and (5-tert-butoxycarbonyl-thiophen-2-ylmethyl)-triphenylphosphonium bromide (29.1 g, 63.4 mmol) were dissolved in DMF (350 mL). DBU was added and the mixture was heated to 80° C. for 35 minutes. The reaction mixture was allowed to cool to room temperature and separated between diethyl ether (3×500 mL) and water (2000 mL). The organic phases were collected and washed with water (1×500 mL). The organic phase was dried (MgSO4) and the solvent was removed in vacuo. The remaining crude material was added heptane (300 mL) and stirred for 30 minutes, filtered and the solvent was removed in vacuo to yield 13.6 g of crude material of an E/Z mixture of 5-(12-methoxycarbonyl-dodec-1-enyl)thiophene-2-carboxylic acid tert-butyl ester. This mixture was dissolved in methanol (200 mL). 2 g of 10% Palladium on carbon (50% wet with water) was added and the mixture was stirred under a hydrogen atmosphere with 10 bar pressure for 90 minutes, filtered and the solvent was removed in vacuo to yield 11.6 g of 5-(12-methoxycarbonyl-dodecyl)-thiophene-2-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796205B2
Source datasetuspto-grants-2014_08
ORD IDord-ea42da1d83754a1981e8ff6a47140ed5
Source noteuspto-grants-2014_08