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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508635Generated: October 30, 2026

Triethylamine → HCID 89975671, compound

https://huagongshe.com/reaction/1508635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 89975670HCID 89975670—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89975671HCID 89975671—

Reaction Conditions

Temperature15 °C

Reaction Steps

3.3 mL of triethylamine was added to a solution of 3.6 g of 5-(methoxyimino)-4-phenoxypentan-2-ol in 36 mL of tetrahydrofuran, and thereafter, 1.2 mL of methanesulfonyl chloride was added to the mixture at a temperature of 0° C. to 10° C. The obtained mixture was stirred at 15° C. or lower for 1 hour. Thereafter, 200 mL of ethyl acetate and 200 mL of water were added to the reaction mixture, and the water layer was then removed. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was then distilled away under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1), so as to obtain 4.4 g of 5-(methoxyimino)-4-phenoxypentan-2-yl methanesulfonate in the form of a light yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221865B2
Source datasetuspto-grants-2015_12
ORD IDord-17c9899436ee4137bda6e527890868a1
Source noteuspto-grants-2015_12