HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Methyl-4-nitropentyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Pentanol, 4-methyl-4-nitro- | HCID 228070 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methyl-4-nitropentyl methanesulfonate | HCID 13047121 | 93.8% |
Reaction Steps
4-Methyl-4-nitropentanol (4.3 g, 29.2 mmol) was dissolved in methylene chloride (100 ml) and triethylamine (6.1 ml, 43.8 mmol) was added, which was followed by ice-cooling. Methanesulfonyl chloride (2.94 ml, 38.0 mmol) was added and the mixture was stirred for 1 h under ice-cooling. The mixture was washed with water (50 ml), 0.5 mol/L hydrochloric acid (50 ml), 5% aqueous sodium hydrogencarbonate solution (50 ml) and saturated brine (50 ml). Methylene chloride was evaporated by concentration under reduced pressure and the residue was subjected to crystallization with ethyl acetate (4 ml) and n-hexane (20 ml). After filtration, the residue was dried under reduced pressure at 40° C. to give the objective compound (6.17 g, yield 93.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664412B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-7824b3405d304f88800ea966dbc8e7f8 |
| Source note | uspto-grants-2003_12 |