HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717969Generated: October 26, 2026
2-Methyl-2-butene → 2-(1-(Tert-butoxycarbonyl)pyrrolidin-3-yl)thiazole-5-carboxylic acid
https://huagongshe.com/reaction/717969
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | Tert-butyl 3-(5-formylthiazol-2-yl)pyrrolidine-1-carboxylate | HCID 86701991 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(1-(Tert-butoxycarbonyl)pyrrolidin-3-yl)thiazole-5-carboxylic acid | HCID 86701992 | — |
Reaction Steps
tert-Butyl 3-(5-formylthiazol-2-yl)pyrrolidine-1-carboxylate (3.65 g, 12.93 mmol) was suspended in water (35 ml) and t-butanol (60 ml). Sodium dihydrogenphosphate (2.094 g, 17.45 mmol) was added, followed by 2-methylbut-2-ene (5.34 ml, 50.4 mmol). After 5 minutes, sodium chlorite (2.92 g, 32.3 mmol) was added in portions over about 5 minutes (mildly exothermic). The reaction was stirred for 1 hour at room temperature, then additional 2-methyl-2-butene (2 mL) was added. After stirring for 2 hours at room temperature, the reaction was concentrated and water (100 mL) was added. The mixture was adjusted to pH 2 by addition of 1N hydrochloric acid, then extracted dichloromethane. The organic extracts were dried over sodium sulfate, filtered and concentrated to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193723B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-3f58e69960d148b0b92990f907f8d11b |
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| Source note | uspto-grants-2015_11 |
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