HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047889Generated: October 30, 2026
Sodium Bicarbonate → 2-[4-Methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1047889
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4,4,5,5-Tetramethyl-2-(2-methylprop-1-en-1-yl)-1,3,2-dioxaborolane | HCID 15148447 | — |
| Reactant | 2-(2-Bromo-4-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester | HCID 59314151 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-Methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid ethyl ester | HCID 59314319 | 92% |
Reaction Steps
A mixture of 2-(2-bromo-4-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (880 mg, 2.2 mmol), 4,4,5,5-tetramethyl-2-(2-methyl-propenyl)-[1,3,2]dioxaborolane (903 μL, 4.4 mmol) and saturated NaHCO3 solution (4.4 mL) in anhydrous DMF (20 mL) is degassed with N2. While under N2 atmosphere, tetrakis(triphenylphosphine)palladium (196 mg, 10 mol %) is added and the reaction is heated in a 110° C. oil bath for 2 h. The reaction is cooled to room temperature, poured into water (40 mL) and extracted with EtOAc (2×30 mL). The combined organic layers are washed with water (15 mL) and brine (20 mL) then concentrated in vacuo. The residue is purified by flash column chromatography (24 g silica gel, gradient elution: 0-50% EtOAc in heptane) to give product (278) as a reddish-brown viscous oil (764 mg, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569535B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-47e3c9d065a242a4952c8c259dfd22cb |
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| Source note | uspto-grants-2013_10 |
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