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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243497Generated: October 31, 2026

Ethyl bromoacetate → HCID 68546571, compound

https://huagongshe.com/reaction/2243497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 68548906HCID 68548906—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11718381HCID 11718381—
ProductHCID 68546571HCID 6854657197%

Reaction Steps

To a solution of 3-methoxycarbonylmethylsulfanyl-benzo[b]thiophene-2,6-dicarboxylic acid 6-allyl ester 2-methyl ester (1.05 g, 2.76 mmol) in DMF was added DBU (0.83 mL, 5.53 mmoL) at room temperature. The resultant mixture was stirred for 24 hours. To this was added ethyl bromoacetate (0.92 mL, 8.28 mmoL) and K2CO3 (1.14 g, 8.26 mmoL). The reaction mixture was stirred for additional 2 hours, then aq. NH4Cl (200 mL and water (300 mL) was added. The white precipate was collected by filtration and washed with water to give the desired compound, 1-ethoxycarbonylmethoxy-3,8-dithia-cyclopenta[a]indene-2,6-dicarboxylic acid 6-allyl ester 2-methyl ester (1.162 g, 97% overall).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674822B2
Source datasetuspto-grants-2010_03
ORD IDord-ca74a27877714583b9a888ab2a34e133
Source noteuspto-grants-2010_03