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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245798Generated: November 2, 2026

Hydroxylamine → 6-(4'-Chloro-biphenyl-4-sulfinyl)-hexanoic acid hydroxyamide

https://huagongshe.com/reaction/2245798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant6-(4'-Chloro-biphenyl-4-ylsulfinyl)-hexanoic acid methyl esterHCID 10067377—
SolventTetrahydrofuranHCID 8028—
Product6-(4'-Chloro-biphenyl-4-sulfinyl)-hexanoic acid hydroxyamideHCID 1031679979%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the 6-(4′-chloro-biphenyl-4sulfinyl)-hexanoic acid methyl ester (400 mg, 1.1 mmol) in distilled THF (10 mL) containing 50% aqueous hydroxylamine (0.65 mL, 9.9 mmol) was added at 0° C. a solution of potassium hydroxide in methanol (1.9 mL, 1M, 1.9 mmol) in a dropwise manner. After stirring at 0° C. for 1 h, distilled water (10 mL) was added and the mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C. The aqueous solution was extracted with ethyl acetate (2×20 mL) and the combined extracts were washed with brine (40 mL), dried over anhydrous MgSO4, filtered and evaporated to dryness. The residue was recrystallised from acetone to give the title compound (315 mg, 79%) as a white powder, mp 108-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683185B2
Source datasetuspto-grants-2010_03
ORD IDord-27d2117e8c0143989482d4f595f770cf
Source noteuspto-grants-2010_03