HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-adamantyl Chloroformate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Adamantanol | HCID 64149 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-adamantyl Chloroformate | HCID 10878537 | — |
Reaction Steps
To a stirred solution of 2-adamantanol (0.912 g, 6 mmol) in dry CH2Cl2 (15 mL) was added bis(trichloromethyl)carbonate (0.653 g), pyridine in dry CH2Cl2 (10 mL) at 0° C. The reaction mixture was warmed to room temperature and stirred for two hours. The solvent was removed in vacuo at 30° C., taken up in ethyl acetate (30 mL) and stirred for 10 minutes. The pyridinium hydrochloride precipitate was filtered off and the solvent removed in vacuo at 30° C., to give an oil which solidified upon standing (1.29 g, 100%). IR (film) 1778 cm-1 ; NMR (CDCl3) δ1.55-1.65 (2H, m), 1.70-1.80 (4H, m), 1.85-1.95 (4H, m), 2.00-2.10 (2H, m), 2.15-2.20 (2H, m), 5.02 (1H, 6, J 3.3 Hz CHOCOCl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580896 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-3e707e1279a34bd2ac9ccdac66487d85 |
| Source note | uspto-grants-1996_12 |