HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222278Generated: October 30, 2026
Sodium hydride → benzyl[(2S)-1,4-dioxan-2-ylmethyl]methylcarbamate
https://huagongshe.com/reaction/222278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | benzyl N-methylcarbamate | HCID 562265 | — |
| Reactant | (2R)-1,4-dioxan-2-ylmethyl methanesulfonate | HCID 86609782 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | benzyl[(2S)-1,4-dioxan-2-ylmethyl]methylcarbamate | HCID 53309827 | — |
Reaction Steps
Sodium hydride (29 mg, 0.74 mmol) was suspended in 2 mL of N,N-dimethylformamide (DMF) and cooled to 0° C. A solution of benzyl methylcarbamate (81 mg, 0.49 mmol) in 2 mL of DMF was added via syringe. After 20 minutes, a solution of (2R)-1,4-dioxan-2-ylmethyl methanesulfonate (191 mg, 0.97 mmol) in 2 mL of DMF was added by syringe and the mixture was heated to 70° C. After 2 h the mixture was cooled to ambient temperature, then diluted in diethyl ether, washed with water and brine, then dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography (silica, ethylacetate/hexanes) to afford the title compound. LRMS (APCI) calc'd for (C14H20NO4) [M+H]+, 266.1; found, 266.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08207186B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-4a4761e39d6742a4b199f7f56a2efcbe |
|---|
| Source note | uspto-grants-2012_06 |
|---|