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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545472Generated: October 26, 2026

Acetic Acid → Benzo[b]thiophene-2,5-dicarboxylic acid 2-tert-butyl ester 5-methyl ester

https://huagongshe.com/reaction/545472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium SulfideHCID 14804—
Reactanttert-Butyl chloroacetateHCID 66052—
ReactantMethyl 3-formyl-4-nitrobenzoateHCID 10867527—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzo[b]thiophene-2,5-dicarboxylic acid 2-tert-butyl ester 5-methyl esterHCID 59556407—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium sulfide (7.95 g, 102 mmol) in anhydrous DMF (200 mL) at 0° C. were added acetic acid (5.80 mL, 102 mmol) and additional DMF (100 mL). The mixture was allowed to stir at 0° C. for 30 min and chloro-acetic acid tert-butyl ester (14.6 mL, 102 mmol) was added followed by additional DMF (50 mL). The resulting mixture was allowed to stir at 0° C. for 30 min and at rt for 30 min. To this mixture were added K2CO3 (16.4 g, 119 mmol) and 3-formyl-4-nitro-benzoic acid methyl ester (17.68 g, 84.55 mmol) in DMF (30 mL). The resulting mixture was heated at 55° C. for 22 h, cooled to rt and poured into water (1.2 L). The solid formed was filtered, washed with water (300 mL) and crystallized from MeOH to give benzo[b]thiophene-2,5-dicarboxylic acid 2-tert-butyl ester 5-methyl ester as a pale solid. MS (EI): cal'd 237.0 (M-tbutyl+H+) exp 237.1 (M-tbutyl+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935724B2
Source datasetuspto-grants-2011_05
ORD IDord-fc977b313a834612b9976ab993c1a22e
Source noteuspto-grants-2011_05