HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330730Generated: October 30, 2026
1-Methylimidazole → HCID 67341044, compound
https://huagongshe.com/reaction/330730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Cyanoethyl N,N-diisopropylchlorophosphoramidite | HCID 2734844 | — |
| Reactant | HCID 68379568 | HCID 68379568 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67341044 | HCID 67341044 | 42.6% |
Reaction Steps
To a cooled solution (0° C.) of 1,4-anhydro-2-O-benzyl-5-O-[bis(4-methoxyphenyl)(phenyl)methyl]D-ribitol (1.60 g, 3.04 mmol) and N,N-diisopropylethylamine (1.59 mL, 9.11 mmol) in DCM (20 mL), 2-cyanoethyl-N,N-diisopropylchlorophosphoramidite (1.44 g, 6.08 mmol) and 1-methylimidazole (0.12 mL, 1.519 mmol) were added. The reaction mixture was warmed to ambient temperature and stirred for 90 min. The reaction was then quenched with methanol (5 mL) and stirred for 5 min. The solvent was then removed in vacuo, and the residue was purified by flash chromatography using 20% ethyl acetate in hexane to obtain 0.94 g (1.293 mmol, 42.6%) of the pure product. LCMS: for C42H51N2O7P calculated 726.3. found 727.3 [M+H]+ and 749.4 [M+Na]+. 31P NMR (400 MHz, CD3CN) δ: 149.94, 149.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08877439B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-57ace1569bf34018b026787b7523477d |
|---|
| Source note | uspto-grants-2014_11 |
|---|