HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389975Generated: October 31, 2026
Diethylethanolamine → 2,2'-oxybis(n,n-diethylethanamine)
https://huagongshe.com/reaction/1389975
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylethanolamine | HCID 7497 | — |
| Reactant | Sulfur trioxide | HCID 24682 | — |
| Product | 2,2'-oxybis(n,n-diethylethanamine) | HCID 283323 | 17.1% |
Reaction Steps
Using the apparatus of Example 1, a solution of 2.43 moles of sodio-2-N,N-diethylaminoethoxide in 4.57 moles of N,N-diethylethanolamine at about 50° C. was added to he reactor. To this mixture was added 514 grams of Diluent II. The resulting mixture was cooled to 25° C. with stirring and then circulated through the scrubber. A vapor mixture of sulfur trioxide and nitrogen, produced by sparging nitrogen gas through liquid sulfur trioxide at a rate of about 148 cubic centimeters per minute, was passed into the gas inlet tube of the reactor over a period of about 2 hours and 10 minutes until 1.01 moles of sulfur trioxide has been added to the reactor, while the stirred mixture in the reactor was maintained at about 24° C. Upon completion of the addition of sulfur trioxide to the reactor, the mixture was stirred for one hour and then heated to a reflux temperature of 110° C. The mixture was refluxed with stirring for 11 hours, and then it was cooled and filtered through a kiesel-guhr-coated filter. The filtrate was distilled through a 35-tray Oldershaw column to give 0.39 moles of bis[2-(N,N-diethylamino)ethyl]ether as a fraction boiling at 120° C. at 15 mm. The yield of bis[2-(N,N-diethylamino)ethyl]ether was 39 percent, based on sulfur trioxide employed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04247482 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-09036c35209d412d8ea0b1c0ecbc4f50 |
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| Source note | uspto-grants-1981_01 |
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