HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799705Generated: October 30, 2026
1-Iodoethyl cyclohexyl carbonate → HCID 131727999, compound
https://huagongshe.com/reaction/1799705
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodoethyl cyclohexyl carbonate | HCID 11109278 | — |
| Reactant | HCID 23668431 | HCID 23668431 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 131727999 | HCID 131727999 | 20,969.6% |
Reaction Steps
A solution (2 ml) of 0.147 mg of 1-(cyclohexyloxycarbonyloxy)ethyl iodide in hexane was added to a solution of 51.8 mg of sodium (1R,5S,6S)-2-[[(Z)-2-[4-(2-hydroxyethoxy)methylthiazol-5-yl]ethen-1-yl]thio]-6-((1R)-1-hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylate in 2 ml of N,N-dimethylacetamide under an argon atmosphere at −10° C. The mixture was stirred at the same temperature for one hr, and 2 ml of hexane was then added to the reaction solution, followed by separation into an upper layer and a lower layer. Brine was added to the lower layer, and the mixture was extracted twice with ethyl acetate. The organic layers were combined, were washed twice with brine, were dried over anhydrous magnesium sulfate, were filtered, and were concentrated under the reduced pressure, and the residue was purified by column chromatography on silica gel (chloroform:methanol=20:1) to give 61.7 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344154B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-0a17e58e3766481da80d5bbab5f6c1fc |
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| Source note | uspto-grants-2013_01 |
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