HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480145Generated: October 30, 2026
2-Methyl-2-butene → HCID 178456483, compound
https://huagongshe.com/reaction/480145
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | HCID 178456482 | HCID 178456482 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178456483 | HCID 178456483 | — |
Reaction Steps
To a solution of [4-(2,6-dioxo-1,3-dipropyl-2,3,6,9-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-acetaldehyde (170 mg, 0.440 mmol) in t-BuOH (10 ml) and 2-methyl-2-butene (10 eq, 4.4 mmol, 470 μL), cooled with the aid of an ice bath, was added NaClO2 (1.5 eq, 0.66 mmol). The resulting yellow solution was allowed to reach ambient temperature over a period of 14 h then concentrated in vacuo. The resulting oily residue was partitioned between water (10 ml) and CH2Cl2 (10 ml). The aqueous phase was acidified by the dropwise addition of concentrated HCl and the resulting precipitate was collected, washed with water and dried to afford 105 mg (59%) as a white powder. 1H NMR (400 MHz, CDCl3); d 0.91 (t, 3H), 0.93 (t, 3H), 1.63 (m, 2H), 1.77 (m, 2H, partially-obscured), 1.82 (m, 6H), 2.01 (m, 6H), 2.32 (s, 2H), 3.95 (m, 2H), 4.07 (m, 2H), 12.74 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649600B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-0932d8ed86604c469d1f6fdf0d3b9db2 |
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| Source note | uspto-grants-2003_11 |
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