HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188541Generated: October 30, 2026
Formaldehyde → 1,8-Diazabicyclo(5.4.0)undec-7-ene
https://huagongshe.com/reaction/2188541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-Naphthalenesulfonic acid | HCID 6812 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Product | Morwet D 425 | HCID 57351120 | — |
Reaction Steps
To a reaction vessel equipped with a stirrer and temperature controller were added 21 parts of naphthalenesulfonic acid and 10 parts of ultrapure water. While keeping the temperature of the system at 80 C under stirring, 8 parts of 37% formaldehyde was added dropwise over 3 hours. After completion of the dropwise addition, the reaction mixture was heated to 105 C and the reaction was continued for 25 hours. Thereafter, the reaction mixture was cooled to room temperature (ca. 25 C) and, while keeping the temperature at 25 C in a water bath, DBU was added gradually to adjust the pH to 6.5 (ca. 15 parts of DBU was used). The solid content was adjusted to 40% by addition of ultrapure water to thereby obtain a 40% aqueous solution of a DBU salt of naphthalenesulfonic acid-formalin condensate (B-2), a polymeric anionic surfactant. In addition, the Mw of (B-2) was 5,000.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324143B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-650565fc7e334f2fba0af1cdd935f0f1 |
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| Source note | uspto-grants-2012_12 |
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