HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23964Generated: October 26, 2026
Formaldehyde → 3-(Hydroxymethyl)-1H-pyrrole-2,5-dione
https://huagongshe.com/reaction/23964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Maleimide | HCID 10935 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-(Hydroxymethyl)-1H-pyrrole-2,5-dione | HCID 21981751 | — |
Reaction Steps
Maleimide (10 g, 0.103 mol) was added to 10 mL of a 37% solution of formaldehyde and 0.31 mL of a 5% solution of NaOH was added. Within 10 minutes all of the maleimide had dissolved and an exothermic reaction proceeded. The solution was stirred for 2 hours where white crystals were observed. The solution was placed in a freezer overnight and the resulting crystals filtered and washed with ice cold ethanol and diethyl ether. The white crystals were purified twice by sublimation. See P. O. Tawney, R. H. Snyder, R. P. Conger, K. A. Leibbrand, C. H. Stiteler, and A. R. Williams J. Org. Chem. 26, 15 (1961). m.p. 104-106° C. (9.77 g, 74.6%). 1H-NMR (Acetone-d6, δ, ppm): 4.96 (2H, —CH2—, s), 5.33 (1H, —OH, s), 6.93 (2H, —CH═CH—, s). 13C-NMR (Acetone-d6, δ, ppm): 60.9 (1C, —CH2—), 135.6 (2C, —CH═CH—), 173.1 (1C, —C═O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855745B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-2e85ceccea8b45fd8b427e35ac4dda20 |
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| Source note | uspto-grants-2005_02 |
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