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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873542Generated: November 2, 2026

2-Methyl-2-butene → HCID 68626053, compound

https://huagongshe.com/reaction/1873542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
ReactantSodium Phosphate, Monobasic, DihydrateHCID 23673460—
ReactantHCID 72338932HCID 72338932—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68626053HCID 6862605399.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Cyclopentyl-5-formyl-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 16b (0.266 g, 0.955 mmol) was dissolved in a solvent mixture of 20 mL of tetrahydrofuran and 10 mL of water. Then sodium dihydrogenphosphate dihydrate (0.448 g, 2.87 mmol), sodium chlorite (0.26 g, 2.87 mmol) and 2-methyl-2-butene (0.24 mL, 2.88 mmol) were added at 0° C. The reaction mixture was stirred at 0° C. for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was concentrated to remove tetrahydrofuran and extracted with ethyl acetate. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 5-cyclopentyl-2-dimethylcarbamoyl-octahydro-cyclopenta[c]pyrrole-5-carboxylic acid 16c (0.28 g, yield 99.6%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304411B2
Source datasetuspto-grants-2012_11
ORD IDord-0c7f5a1c2f6f4938968999081fa70d7c
Source noteuspto-grants-2012_11