HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminoheptane → HCID 19107601, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminoheptane | HCID 5603 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(Bromomethyl)benzenesulfonyl chloride | HCID 2734409 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19107601 | HCID 19107601 | 39% |
Reaction Steps
To a solution of 2-aminoheptane (1.67 ml, 0.011 mol) and triethylamine (1.55 ml, 0.011 mol) in dry THF (100 ml) was added powdered 4-bromomethylbenzenesulphonyl chloride (3.0 g, 0.011 mol) in one portion. The mixture was stirred for 3 h at room temperature. The reaction mixture was treated with saturated ammonium chloride (60 ml) , extracted with ethyl acetate (3×80 ml), the organics combined and washed with water (50 ml) and brine (50 ml), dried over anhydrous sodium sulphate, filtered and evaporated. The resulting oil was purified by chromatography (silica: 1:2 hexane:ethyl acetate) to give N-1-methylhexyl 4-bromomethylbenzenesulphonamide (1.45 g, 39%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05276153 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-656734927bcc42ed9c24534f1ac78f56 |
| Source note | uspto-grants-1994_01 |