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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193762Generated: November 2, 2026

Salicylamide → 2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamide

https://huagongshe.com/reaction/1193762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylamideHCID 5147—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantSodium amideHCID 24533—
Reactant1-Methyl-3-pyrrolidinolHCID 93074—
ReactantSodium MethoxideHCID 10942334—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamideHCID 13726283—

Reaction Conditions

Temperature70 °C

Reaction Steps

To 85.6 g (2.2 moles) of sodium amide in 1.5 liter of dry toluene was added 202 g (2 moles) of 1-methyl-3-pyrrolidinol so as not to exceed a temperature of 50° C. The mixture was then heated to 70° C. for 4.5 hours. The mixture was cooled and 381 g (2 moles) of o-toluenesulfonylchloride was added at a rapid drop while maintaining a temperature of 20°-30° C. with an ice bath. The mixture was stirred at room temperature for 2.5 hours and washed with water. The toluene solution was dried with sodium sulfate and concentrated. The residue, dissolved in 500 ml of dimethylformamide, was added to a reaction mixture prepared by adding 119 g (2.2 moles) of sodium methoxide and 274 g (2.0 moles) of salicylamide to one liter of dimethylformamide and the mixture was worked up as in preparation 1. Yield of product was 170 g (38%), m.p. 116°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04810795
Source datasetuspto-grants-1989_03
ORD IDord-75d1c689499c4e6880ac1efad5654495
Source noteuspto-grants-1989_03