HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 86761809, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-butyl ((2R,3R)-1-hydroxy-3-methoxybutan-2-yl)carbamate | HCID 11816842 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86761809 | HCID 86761809 | — |
Reaction Steps
To an ice cold solution of ((1R,2R)-1-hydroxymethyl-2-methoxy-propyl)-carbamic acid t-butyl ester (5 g, 22 mmol) in DMSO (20 mL) and DCM (250 mL) was added DIEA (12 mL, 69 mmol), followed by dropwise addition of a solution of Py.SO3 (11 g, 69 mmol) in DMSO (50 mL, +20 mL to rinse the funnel). The reaction mixture was stirred at rt for 5 h. After removal of the DCM, the residue was diluted with Et2O (400 mL) and washed with H2O (2×100 mL) and brine (150 mL). The aqueous layer was back extracted with Et2O (100 mL). The combined Et2O layer was washed with saturated NaHCO3 (150 mL) and dried (Na2SO4). The solvent was removed to give the titled compound. MS (MH+ 218).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426414B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-5badb49867d94150af90ab312493318f |
| Source note | uspto-grants-2013_04 |