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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197910Generated: November 1, 2026

N-Methyl-D-glucamine → HCID 14766065, compound

https://huagongshe.com/reaction/1197910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-D-glucamineHCID 8567—
ReactantAcryloyl chlorideHCID 13140—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 18649787HCID 18649787—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 14766065HCID 1476606541%

Reaction Steps

N-methyl-1-amino-1-deoxy-D-glucitol (0.5 mol, 97.6 g) was dissolved in about 300 ml of water. Then 1-2 g of sodium nitrite was added and the solution was cooled in an ice bath. Potassium hydroxide (0.6 mole) was dissolved in water and cooled. Acryloyl chloride (0.55 mole) was mixed with an equal volume of methylene chloride. The reaction was done in the same way as described in step 3 for the synthesis of N-acryloyl-2-amino-2-deoxy-D-glucitol. The salts were also removed as described above. However, even after several weeks long evaporation from a crystallization dish, the product was not dry. After addition of more polymerization inhibitor, drying was continued in a desiccator. The semi-dry mass (yield 41-60%) was dissolved in warm dioxane which contained p-methoxy phenol. The warm solution was filtered through Celite and upon cooling the crystals were formed. They were collected and recrystallized from dioxane. The title compound is very hygroscopic.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05278270
Source datasetuspto-grants-1994_01
ORD IDord-525c038ba6604ce281df31ac4a739575
Source noteuspto-grants-1994_01