HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662047Generated: October 29, 2026
Methanol → ethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylate
https://huagongshe.com/reaction/1662047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl 5-formyl-1,4-dimethyl-1H-pyrrole-2-carboxylate | HCID 59454108 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylate | HCID 59454025 | 66% |
Reaction Steps
To a mixture of ethyl 5-formyl-1,4-dimethyl-1H-pyrrole-2-carboxylate (0.99 g) and methanol (10 ml) was added sodium borohydride (0.38 g) under ice-cooling, followed by stirring for 5 minutes under ice-cooling. To a reaction mixture was added a saturated aqueous ammonium chloride solution under ice-cooling, followed by stirring at room temperature for 0.5 hour. To the reaction mixture were added water and ethyl acetate, and the aqueous layer was separated and extracted with ethyl acetate. The organic layer was combined, washed with a saturated sodium bicarbonate solution and saturated brine in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4:1) to obtain ethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylate (0.66 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030489B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c7b63308f5d74e49b665a7c9fdaa6c1c |
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| Source note | uspto-grants-2011_10 |
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