HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Thiomorpholine, N-BOC protected
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | tert-Butoxycarbonyl dicarbonate | HCID 86600350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Thiomorpholine, N-BOC protected | HCID 21949316 | 96.2% |
Reaction Steps
Thiomorpholine (5.0 ml, 53 mmol) was dissolved in tetrahydrofuran (200 ml); triethylamine (8.1 ml, 58 mmol) was added thereto; and the reaction mixture was stirred at room temperature. tert-Butoxycarbonyl dicarbonate (13.3 ml, 58 mmol) was added thereto and the reaction mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated under reduced pressure; and the residue was purified by silica gel column (eluent; hexane:ethyl acetate=from 80:20, 75:25 to 70:30) to yield the title compound as colorless crystals (10.4 g, 51 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468380B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-1291f0e48b6f454687c05243ca8ecd72 |
| Source note | uspto-grants-2008_12 |