Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204233Generated: October 30, 2026

Benzoic acid, 4-fluoro-, ethyl ester → HCID 70518106, compound

https://huagongshe.com/reaction/2204233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 4-fluoro-, ethyl esterHCID 67976—
ReactantHCID 178455544HCID 178455544—
SolventDimethylformamideHCID 6228—
ProductHCID 70518106HCID 70518106—

Reaction Conditions

Temperature80 °C

Reaction Steps

Ethyl 4-fluorobenzoate (5.00 g, 29.7 mmol) and tert-butylsulfanylsodium (6.67 g, 59.5 mmol) were combined in DMF (50 mL). The reaction mixture was heated at 80° C. for 67 hours. The reaction mixture was partitioned between ethyl acetate (100 mL) and water (100 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers were dried over sodium sulfate, filtered and the solvent was evaporated under reduced pressure to yield ethyl 4-tert-butylsulfanylbenzoate. The aqueous layer was acidified with hydrochloric acid. The aqueous layer was extracted with ethyl acetate (3×100 mL), and the combined organic layer was washed with water (1×50 mL) and brine (1×50 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was evaporated under reduced pressure to yield 4-(tert-butylthio)benzoic acid as an off-white solid. 1H NMR (400 MHz, DMSO) δ 13.10 (s, 1H), 7.93 (d, J=8.2 Hz, 2H), 7.61 (d, J=8.2 Hz, 2H), 1.28 (s, 9H). ESI-MS m/z calc. 210.1, found 211.1 (M+1)+; Retention time: 1.64 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365588B2
Source datasetuspto-grants-2016_06
ORD IDord-720065fe115041b69f2557e6b4dbc023
Source noteuspto-grants-2016_06