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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508665Generated: October 31, 2026

Methanol → HCID 118120854, compound

https://huagongshe.com/reaction/1508665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 118108777HCID 118108777—
SolventTriethylamineHCID 8471—
ProductHCID 118120854HCID 118120854102%

Reaction Steps

8.0 mL of methanol and 712 mg of O-methylhydroxylamine hydrochloride were added to 1.5 g of 5-methyl-3-(pyridin-2-ylsulfanyl)oxolan-2-ol, and thereafter, 1.1 mL of triethylamine was added dropwise to the mixture. The thus obtained mixture was stirred at room temperature for 2 hours. Thereafter, the solvent was distilled away under reduced pressure, 50 mL of ethyl acetate and 50 mL of water were then added to the residue, and the water layer was then removed. The organic layer was washed with a saturated sodium chloride aqueous solution, and was then dried over anhydrous magnesium sulfate. After that, the solvent was distilled away under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/acetone=4/1), so as to obtain 1.74 g of 5-(methoxyimino)-4-(pyridin-2-ylsulfanyl)pentan-2-ol in the form of a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221865B2
Source datasetuspto-grants-2015_12
ORD IDord-3a0ee735cf3148e2a900789a2c726c82
Source noteuspto-grants-2015_12