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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518300Generated: November 1, 2026

Sodium Thiosulfate → 2-Bromo-4-(ethylsulfonyl)-1-fluorobenzene

https://huagongshe.com/reaction/518300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant(3-Bromo-4-fluorophenyl)(ethyl)sulfaneHCID 86704956—
SolventDichloromethaneHCID 6344—
Product2-Bromo-4-(ethylsulfonyl)-1-fluorobenzeneHCID 5852197550%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115114B2
Source datasetuspto-grants-2015_08
ORD IDord-c8d210d2c33f4505a36f586e6ce4a014
Source noteuspto-grants-2015_08