Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356199Generated: November 1, 2026

Tetrahydrothiophene → HCID 86604150, compound

https://huagongshe.com/reaction/2356199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrothiopheneHCID 1127—
Reactant1,4-Bis(bromomethyl)-2,5-bis(trifluoromethyl)benzeneHCID 59260576—
SolventMethanolHCID 887—
ProductHCID 86604150HCID 86604150—

Reaction Conditions

Temperature50 °C

Reaction Steps

Tetrahydrothiophene (0.27 mL, 3 mmol) was added to a suspension of compound 24 (200 mg, 0.5 mmol) in dry methanol (5 mL). The solid was dissolved to form a clear solution within 10 min. This solution was filtered via 0.45 μm membrane filter and then heated to 50° C. with stirring for 24 h. After cooling down to room temperature, the solvent was completely removed in vacuo and cold acetone (10 mL) was added to the residue. The precipitate was then filtered and dried to give compound 217a as a colorless, hygroscopic solid (192 mg, 67%): 1H NMR (300 MHz, D2O): 8.17 (2H, s), 4.76 (4H, s), 3.52-3.62 (8H, m), 2.34-2.47 (8H, m); 19F NMR (282 MHz, D2O): −60.2; HR-MS (EI) calcd. for C18H22F6S2Br2 (M+): 573.94, found ([M-Br]+): 495.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759127B2
Source datasetuspto-grants-2010_07
ORD IDord-5fcb0f356f6b4421be5c0e8843522cc6
Source noteuspto-grants-2010_07