HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364677Generated: October 25, 2026
Hydrochloric Acid → N,N-Diethylacrylamide
https://huagongshe.com/reaction/364677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Methyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate | HCID 12271748 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-Diethylacrylamide | HCID 17583 | — |
Reaction Steps
7.2 parts 30% methanolic Na-methylate solution are added to 36.5 parts diethylamine. 77 parts 2-carbomethoxy-7-oxabicyclo(2,2,1)hept-5-ene are added drop-wise at 40° C. The reaction medium is then stirred for 15 hours at this temperature and neutralised with 4 parts concentrated hydrochloric acid. 100 parts methylene chloride and 50 parts water are added, the organic phase separated off, and the aqueous phase extracted 3 times with 25 parts methylene chloride in each instance. The combined organic phases are reduced in a rotary evaporator at a bath temperature of 90° C. and under a vacuum of 20 Torr. The residue is heated under a vacuum of 20 Torr to 110° to 120° C. (bath temperature 140° C.). On conclusion of the furane separation, the sedimentation temperature increases and the product distills over at the now lowered pressure. 21 parts N,N-diethylacrylamide with a boiling point of 55° C. at 1 Torr are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04605740 |
|---|
| Source dataset | uspto-grants-1986_08 |
|---|
| ORD ID | ord-26fbb501dc83464bbb6d1b5292d80de1 |
|---|
| Source note | uspto-grants-1986_08 |
|---|