HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-Bromo-4-(ethylsulfonyl)-1-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | (3-Bromo-4-fluorophenyl)(ethyl)sulfane | HCID 86704956 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-4-(ethylsulfonyl)-1-fluorobenzene | HCID 58521975 | 50% |
Reaction Steps
To 2-bromo-4-ethylsulfanyl-1-fluorobenzene (2.2 g, 9.36 mmol) in DCM (20 mL) was added m-CPBA (6.47 g, 37.4 mmol). The mixture was stirred at room temperature for 12 h. Aqueous saturated Na2S2O3 (100 mL) was added, and extractive work up with CH2Cl2 gave the title compound (1.5 g, 50%) as a yellow solid which was carried on without purification. 1H NMR (CDCl3, 400 MHz) δ 8.15 (dd, J1=6.4 Hz, J2=2.4 Hz, 1H), 7.88-7.85 (m, 1H), 7.32 (t, J=8.4 Hz, 1H), 3.14 (q, J=7.2 Hz, 2H), 1.31 (t, J=7.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034900B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-a46cb9c37d7048e4b7622c7e09bf72b0 |
| Source note | uspto-grants-2015_05 |