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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896182Generated: November 2, 2026

Sodium Carbonate → HCID 86762017, compound

https://huagongshe.com/reaction/1896182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantLithium ChlorideHCID 433294—
Reactantmethyl 5-bromo-1-benzothiophene-2-carboxylateHCID 2824065—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86762017HCID 86762017165.9%

Reaction Steps

1.1 g of tert-butyl 4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylate (purity 70%), 0.7 g of methyl 5-bromobenzo[b]thiophene-2-carboxylate, 0.15 g of PalladiumTetrakis (PdP(Ph3)4), 5.5 ml of 2M sodium carbonate solution and 0.42 g of lithium chloride are placed in 30 ml of DME in a round-bottomed flask under a stream of nitrogen. The mixture is heated at the reflux temperature for 3 hours. The solvent is evaporated off and the residue is dissolved in 35 ml of ethyl acetate. This solution is washed with 2M sodium carbonate solution. The organic phase is dried over Na2SO4, filtered and evaporated under vacuum. 1.6 g of an oily material are isolated, and this material is purified by flash chromatography on a Biotage® column, using 98/2 cyclohexane/ethyl acetate as eluent. 0.45 g of a yellowish solid is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518947B2
Source datasetuspto-grants-2013_08
ORD IDord-c2bc2b0decb74136a82ddf02af67034c
Source noteuspto-grants-2013_08