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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023347Generated: October 31, 2026

Thioglycolic Acid → HCID 67327651, compound

https://huagongshe.com/reaction/1023347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
ReactantLithium HydroxideHCID 3939—
ReactantHCID 70944787HCID 70944787—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67327651HCID 67327651—

Reaction Steps

To a solution of tert-butyl 4-[4-(2-{(4-methoxyphenyl)[(2-nitrophenyl)sulfonyl]-amino}ethyl)benzyl]piperazine-1-carboxylate in DMF (35 mL) was added mercaptoacetic acid (1.35 mL) and LiOH (1.63 g) at room temperature, then the reaction mixture was stirred over night. The reaction mixture was added mercaptoacetic acid (1.35 mL) and LiOH (1.63 g), and stirred for 5 hours. The reaction mixture was diluted with H2O, and extracted with AcOEt. The organic layer was washed with water and saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=1/1 to 1/2) to afford tert-butyl 4-(4-{2-[(4-methoxyphenyl)amino]ethyl}benzyl)piperazine-1-carboxylate as a pale yellow amorphous (5.96 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-2b68b5c3907b4802858b60f78893844e
Source noteuspto-grants-2014_05