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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515549Generated: October 28, 2026

Acetic Acid → HCID 89619548, compound

https://huagongshe.com/reaction/515549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantDimethyl CarbonateHCID 12021—
ReactantSodium MethoxideHCID 10942334—
ReactantBenzeneacetic acid, 3,5-dichloro-, methyl esterHCID 67195643—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 89619548HCID 8961954885%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture sodium methoxide in methanol (28.46 g, 25%, 0.132 mol) and toluene (150 mL) was boiled with provision of a five plate Oldershaw column to remove the methanol/toluene azeotrope. The mixture was cooled to 60° C. and toluene (a volume equal to the total volume of the distillate) was added to the mixture. Dimethyl carbonate (35.95 g, 0.399 mol) was added to the reaction mixture. Methyl 3,5-dichlorobenzeneacetate (i.e. the product from Step A1b) (22.2 g, 0.101 mol) in toluene (17 mL) was added to the mixture over 70 min. When the addition was complete the mixture was stirred for a further 60 min at 60° C. The mixture was boiled and the dimethyl carbonate/methanol azeotrope was removed using the Oldershaw column. The mixture was cooled to 25° C. and acetic acid (9.5 g, 0.158 mol) was added dropwise. Water (100 mL) was added to the mixture and the organic phase separated and removed under reduced pressure. Crystallisation of the resulting residue from methanol (36 mL) gave the product as a white solid (23.9 g, 85%) melting at 72-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108965B2
Source datasetuspto-grants-2015_08
ORD IDord-ae1dbd4fa707460fbd36eaa09c3c2d58
Source noteuspto-grants-2015_08