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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576976Generated: November 4, 2026

Triethylamine → HCID 352955, compound

https://huagongshe.com/reaction/1576976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-hydroxybenzenecarboximidoyl chlorideHCID 2756315—
SolventDiethyl EtherHCID 3283—
ProductHCID 352955HCID 35295536.8%

Reaction Steps

The 9.4 g of recovered benzohydroximoyl chloride was dissolved in 100 ml of anhydrous ether and the solution was cooled to -20°. To the cold solution was rapidly added 12.3 g of triethylamine. To this mixture was slowly added (during 45 minutes) a solution of 6.95 g of methanesulfonyl chloride in 50 ml of anhydrous ether. The mixture was stirred at -30° for 1 hour, then at ambient temperature for about 16 hours. The mixture was filtered and the filtrate was conconcentrated under reduced pressure to give a yellow solid. The solid was recrystallized from a benzene-hexane mixture to give 5.2 g of N-(methanesulfonyloxy)benzimidoyl chloride, m.p. 106°-108°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03983246
Source datasetuspto-grants-1976_09
ORD IDord-d652e83444654308bede2657cf553512
Source noteuspto-grants-1976_09