HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33494Generated: October 26, 2026
Dimethylbarbituric acid → 4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenol
https://huagongshe.com/reaction/33494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylbarbituric acid | HCID 69860 | — |
| Reactant | 1-[2-(4-Allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazole | HCID 22242085 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenol | HCID 22242075 | 97.5% |
Reaction Steps
A solution of 1.00 g (3.43 mmol) 1-[2-(4-allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazole in 60 ml dichloromethane was added to a solution of 1.61 g (10.3 mmol) 1,3-dimethylbarbituric acid and 102 mg (0.09 mmol) Pd(PPh3)4 in 30 ml dichloromethane and stirred for 5 h at 50° C. The mixture was extracted with 3×50 ml sat. NaHCO3-solution and 20 ml water. The organic phase was discarded and the aqueous phase acidified with 2M HCl to pH=4, concentrated to a volume of 50 ml and adjusted to pH=1. After five extractions with ethyl acetate, the organic extracts were combined and dried over MgSO4. After evaporation the residue was purified by chromatography on silica gel (dichloromethane/methanol 100:2) to yield 0.84 g (97%) of 4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429605B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-d9c2db7229934015a6ccd109b303a010 |
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| Source note | uspto-grants-2008_09 |
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