HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanesulfonyl chloride → Butane-1-sulfonic acid 6-chloro-2-oxo-2H-1-benzopyran-4-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanesulfonyl chloride | HCID 75430 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloro-4-hydroxycoumarin | HCID 54686348 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Butane-1-sulfonic acid 6-chloro-2-oxo-2H-1-benzopyran-4-yl ester | HCID 11301544 | 25.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
6-Chloro-4-hydroxycoumarin (0.455 mmol, 0.090 g) is suspended in 5 mL DCM. DIEA (1.37 mmol, 0.237 mL) is added and the reaction is cooled to 0° C. 1-Butanesulfonyl chloride (0.5 mmol, 64.8 μL) is dissolved in DCM is added and and the reaction is stirred at ambient temperature for 2 hrs. The DCM is removed under reduced pressure and the residue is redissolved in MeOH/H2O then is purified by HPLC to afford the title compound (36.2 mg, 25%) 1H NMR (DMSO-d6, 300 MHz) δ 7.81 (2H, m), 7.56 (1H, d, J=8.75 Hz), 6.59 (1H, s), 3.99 (2H, m), 1.83 (2H, m), 1.46 (2H, m), 0.92 (3H, t, J=7.25 Hz); MS (ESI, Pos.) calcd for C13H13ClO5S m/z [M+H]=317.0, found 317.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538233B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-dc392f59e2324e7bb409672b481f6f57 |
| Source note | uspto-grants-2009_05 |