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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904763Generated: October 31, 2026

Butyl 6-isocyanatohexanoate → HCID 19848120, compound

https://huagongshe.com/reaction/1904763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl 6-isocyanatohexanoateHCID 13836475—
ReactantHCID 54703303HCID 54703303—
CatalystDabcoHCID 9237—
SolventAcetonitrileHCID 6342—
ProductHCID 19848120HCID 1984812093.4%

Reaction Steps

10.0 g of 2,5-bis-(isopropoxycarbonyl)-3-methyl-4-hydroxythiophene, 20 ml of anhydrous acetonitrile, 15 g of butoxycarbonylpentyl isocyanate (b.p. 149°-151°/ 13 millibar) and 100 mg of triethylene diamine are maintained at 100° C. for 18 hours. The mixture is diluted with 20 ml of acetonitrile. To remove the excess butoxycarbonylpentyl isocyanate, the reaction mixture is shaken three times with 50 ml of ligroin in each case. The acetonitrile phase is evaporated in vacuo. The evaporation residue is dried at 100° C./0.1 mbar. 16.3 g of 2,5-bis-(isopropoxycarbonyl)-3-methyl-4-[5-(butyloxycarbonyl)pentylaminocarbonyloxy]-thiophene are obtained as a viscous material. 1H--NMR 80 MHz CDCL3 δ-values OCH 2H m 5.0-5.5 ppm; OCH2 2H t 4.13 ppm; N--CH2 2H m 3.1-3.5 ppm; hetar-CH3 s 2.39 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839381
Source datasetuspto-grants-1989_06
ORD IDord-34fad4eeecef4f65abb1fc89f19c5695
Source noteuspto-grants-1989_06