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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250920Generated: November 3, 2026

Hydrogen Peroxide → HCID 86586091, compound

https://huagongshe.com/reaction/1250920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantHCID 11186284HCID 11186284—
SolventMethanolHCID 887—
ProductHCID 86586091HCID 8658609124%

Reaction Steps

2-(4-But-2-ynyloxy-phenylsulfanyl)-octanoic acid hydroxamide (prepared in Example 6) (1.78 g, 5 mmol) was dissolved in methanol (50 ml) and H2O2 (30%, 10 ml) was added. The reaction mixture was stirred at room temperature for 96 hours and quenched with ice cold solution of NaHSO3 solution. The reaction mixture was concentrated under reduced pressure and the residue was extracted with chloroform. Examination of the reaction mixture showed the formation of two diastereo isomers and they were separated by silica-gel column chromatography by eluting it with 50% ethyl acetate; hexane. 411 g of (S)-2-[(R)-4-but-2-ynyloxy-phenylsulfinyl)-octanoic acid hydroxamide was isolated as a white solid, mp 132.3° C.; Yield 24%; MS: 352.0 (M+H)+; 1H NMR (300 MHz, DMSO-d6): δ0.834 (m, 3H), 1.19 (m, 9H), 1.76 (m, 1H), 1.84(t, 3H), 3.11-3.17 (dd, 2H), 3.33 (t, 3H), 4.81 (d, 2H) 7.15 (d, J=2.8, 2H), 7.36 (d, J=2.3, 2H), 9.00 (s, 1H), 10.56 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340691B1
Source datasetuspto-grants-2002_01
ORD IDord-6976dfb69fac46ddb3ea821b3fff5793
Source noteuspto-grants-2002_01