HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267483Generated: October 30, 2026
Carbon Dioxide → N-[3-(Dimethylamino)-1,1-dimethylbutyl]-2-propenamide
https://huagongshe.com/reaction/267483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21514639 | HCID 21514639 | — |
| Product | N-[3-(Dimethylamino)-1,1-dimethylbutyl]-2-propenamide | HCID 20432749 | — |
Reaction Steps
A mixture of 144.7 parts (0.63 mole) of N-(1,1-dimethyl-3-dimethylaminobutyl)-3-methoxypropionamide, 1 part of solid sodium hydroxide and 1 part of hydroquinone is charged to a reaction flask fitted with a condenser with a Dry Ice-cooled receiver, a stirrer and temperature control means. The pressure in the flask is reduced to less than 5 mm. and the flask is heated to 80° C. Vigorous reaction begins and liquid condenses in the receiver. After about one-half hour, the temperature is increased to 90° C. and this temperature is maintained for 3 hours. The product is distilled and the desired N-(1,1-dimethyl-3-dimethylaminobutyl)acrylamide is obtained at 80°-91° C./0.3-0.4 mm. The yield is 109.1 parts, or 87.4% of the theoretical amount, and the nitrogen percentage is the calculated 14.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03943114 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-bbbdcf249d1348b1a927a198314ea3ff |
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| Source note | uspto-grants-1976_03 |
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