HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium triacetoxyborohydride → Tert-butyl (4-(oxetan-3-yl)morpholin-2-yl)methylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Reactant | tert-Butyl [(morpholin-2-yl)methyl]carbamate | HCID 19081107 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl (4-(oxetan-3-yl)morpholin-2-yl)methylcarbamate | HCID 86647912 | — |
Reaction Steps
To a solution of tert-butyl morpholin-2-ylmethylcarbamate (0.50 g) in dichloromethane (5 mL) was added oxetan-3-one (0.20 g). After stirring for 5 minutes, sodium triacetoxyborohydride (0.735 g) was added. After stirring for 2 hours, the reaction was diluted with dichloromethane (50 mL) and quenched with saturated NaHCO3 solution (50 mL). The organic layer was separated, washed with brine (40 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (Reveleris 80 g) eluting with a gradient of 0.5% to 5% methanol/dichloromethane over 40 minutes (flow=40 ml/minute) gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029404B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-ba4909475ec24eedaed5a7bbcd0c3789 |
| Source note | uspto-grants-2015_05 |