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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244112Generated: November 2, 2026

Sodium Hydroxide → 2-(benzo[d][1,3]dioxol-5-yl)-N-methoxy-N-methylacetamide

https://huagongshe.com/reaction/2244112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
ReactantBenzo-1,3-dioxole-5-acetic acidHCID 76115—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantBenzo(1,3)dioxol-5-yl-acetyl chlorideHCID 2756584—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product2-(benzo[d][1,3]dioxol-5-yl)-N-methoxy-N-methylacetamideHCID 1491816195.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Thionyl chloride (39.6 g) and a drop of dimethylformamide were added to a solution of benzo(1,3)dioxol-5-yl-acetic acid (30.0 g) in toluene (200 ml) and then the mixture was stirred for 2.5 hours at 60° C., after distilling out the solvent, to yield unpurified benzo(1,3)dioxol-5-yl-acetyl chloride. A solution of sodium hydroxide (20.0 g) in water (150 ml) was added to a solution of N,O-dimethylhydroxylamine hydrochloride (19.5 g) in toluene (200 ml) at 0° C., and further the unpurified benzo(1,3)dioxol-5-yl-acetyl chloride was added thereto, and then the mixture was stirred for 3 hours. The reaction mixture was extracted with toluene and dried over anhydrous magnesium sulfate, and from which the solvent was evaporated to yield unpurified 2-benzo(1,3)dioxol-5-yl-N-methoxy-N-methylacetoamide (35.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678810B2
Source datasetuspto-grants-2010_03
ORD IDord-7c2591c86c8e4bcf9c12c9c670fca1e6
Source noteuspto-grants-2010_03