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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619609Generated: November 1, 2026

Oxalyl chloride → 3-(3-Fluoro-4-methoxy-phenysulfanyl)-3-methyl-butyroyl chloride

https://huagongshe.com/reaction/619609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-(3-Fluoro-4-methoxy-phenylsulfanyl)-3-methyl-butyric acidHCID 21846649—
SolventBenzeneHCID 241—
Product3-(3-Fluoro-4-methoxy-phenysulfanyl)-3-methyl-butyroyl chlorideHCID 1792181788.2%

Reaction Steps

To a solution of 3-(3-fluoro-4-methoxy-phenylsulfanyl)-3-methyl-butyric acid (Compound 201, 3.00 g, 11.6 mmol) in 40 mL of benzene at room temperature was added a solution of oxalyl chloride (2.21 g, 17.4 mmol) in 5 mL of benzene over 30 minutes. After 3 hours, the solution was washed with ice cold 5% aqueous NaOH (CAUTION: a large volume of gas is released during this procedure), followed by ice cold H2O, and finally saturated aqueous NaCl. The solution was dried (Na2SO4) and concentrated under reduced pressure to give 2.83 g of a clear yellow oil. This material was used without further purification in the next step. 1H NMR (300 MHz, CDCl3)δ: 7.27 (2H, m), 6.96 (1H, t, J=8.4 Hz), 3.93 (3H, s), 3.13 (2H, s), 1.42 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05958954
Source datasetuspto-grants-1999_09
ORD IDord-f044985a401f4b4b9c9c8b2a8f2b5542
Source noteuspto-grants-1999_09