HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081536Generated: October 26, 2026
N-Methyl-D-glucamine → N-(2-ethylhexyloxycarbonyl)-N-methyl-D-glucamine
https://huagongshe.com/reaction/1081536
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methyl-D-glucamine | HCID 8567 | — |
| Reactant | 2-Ethylhexyl chloroformate | HCID 62783 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-ethylhexyloxycarbonyl)-N-methyl-D-glucamine | HCID 9924600 | 50% |
Reaction Steps
In a reactor, 117 g (0.6 mol) of N-methyl-D-glucamine were dissolved in a mixture of 800 ml of water and 400 ml of tetrahydrofuran, and 201.6 g (2.4 mol) of sodium hydrogen carbonate were then dispersed. While the temperature of the reaction mixture was maintained at 5° C., 115.6 g (0.6 mol) of 2-ethylhexyl chloroformate were added dropwise, and the mixture was then allowed to react for 3 hours with stirring at 5° C. and left standing overnight at room temperature. The reaction mixture was then filtered and concentrated; the pasty residue obtained was dissolved in 2 liters of acetone and then filtered after cooling to 5° C. The crystallized product collected was dried. 105 g (50% yield) of N-(2-ethylhexyloxycarbonyl)-N-methyl-D-glucamine, the melting point of which is 74° C., were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587169 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-774e7cff87054fc098cc64b519894e8d |
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| Source note | uspto-grants-1996_12 |
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