HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049229Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 86736920, compound
https://huagongshe.com/reaction/2049229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 20344782 | HCID 20344782 | — |
| Reactant | HCID 86736921 | HCID 86736921 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86736920 | HCID 86736920 | — |
Reaction Steps
Equivalent amouts (0.05 mole) of the sodium salt of 4-hydroxy-3-(methoxymethyl)benzeneacetic acid and 6-amino-6-methoxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]-heptane-2-carboxylic acid, ethyl ester, are added to dimethylformamide (DMF). The temperature is maintained at 0° C. Then about 1.2 equivalents of dicyclohexylcarbodiimide in DMF is added. The mixture is stirred at 0° C. for from 0.5 to 3 hours and an additional 2 to 5 hours at room temperature. Filtration of the reaction mixture removes the formed dicyclohexylurea. The filtrate is then diluted with chloroform, methylene chloride or ethyl acetate, washed with water, dried and evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04197240 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-160341866dd246de9141e906f55d678e |
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| Source note | uspto-grants-1980_04 |
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