HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282860Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 21533415, compound
https://huagongshe.com/reaction/1282860
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2H-Thieno(2,3-c)(1)benzopyran-9-ol, 1,4-dihydro-7-(1,2-dimethylheptyl)-1,4,4-trimethyl- | HCID 3043881 | — |
| Reactant | 4-(Piperidin-1-yl)butanoic acid hydrochloride | HCID 13172081 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21533415 | HCID 21533415 | — |
Reaction Steps
A combination of 2.4 g. (6.4 mmole) of 1,2-dihydro-9-hydroxy-7-(3-methyl-2-octyl)-1,4,4,-trimethyl-4H-thieno[2,3-c][1]benzopyran, 1.33 g. (6.4 mmole) of γ-piperidinobutyric acid hydrochloride, 1.40 g. (6.75 mmole) of dicyclohexylcarbodiimide and 125 ml. of methylene chloride was stirred at room temperature for 18 hours. The reaction mixture was cooled and the byproduct of dicyclohexylurea was removed by filtration. The methylene chloride was distilled off on a rotary evaporator to give a colorless, foamy residue, which was purified on 80 g. of magnesium silicate (60-100 mesh) using a graded methanol/chloroform solvent system. The fractions were monitored by thin layer chromatography, and the appropriate fractions were combined to give 1.23 g. (37%) of the desired material as a golden gum. The infrared and nuclear magnetic resonance spectra were in agreement with the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03972880 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-bfb38c029c95459eac970fec468e54cb |
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| Source note | uspto-grants-1976_08 |
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