HuagongsheHuagongshe Chemistry Print Report · For research reference only
(+-)-2-Butanol → HCID 21922929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (+-)-2-Butanol | HCID 6568 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21922929 | HCID 21922929 | 50% |
Reaction Steps
2,6-dichloropurine (5.3 mmol), 2-Butanol (9.01 mmol), triphenylphosphine (7.95 mmol) in 40 ml anhydrous tetrahydrofuran, to which was added drop-wise diisoproplyazidodicarboxylate (7.95 mmol) at room temperature over a period of 30 minutes. The reaction mixture was stirred at room temperature for 24 hrs. The reaction is monitored by TLC or LC/MS. The reaction mixture was poured in to a beaker containing ice-cold water. Extraction of the aqueous layer, using 3×100 ml portions of ethyl acetate, afforded the crude product. This was purified on the silica gel column (10-80% ethyl acetate in petroleum ether, gradient elution), to give the desired compound in a yield of 50%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247410B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-8a63171e41b24b4da9b10ce508a0948a |
| Source note | uspto-grants-2012_08 |