HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434425Generated: October 26, 2026
Triethylamine → 1-Methacryloylindoline-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/434425
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Ethyl Indoline-2-carboxylate | HCID 11949691 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Methacryloylindoline-2-carboxylic acid ethyl ester | HCID 12764222 | — |
Reaction Steps
To a chilled and stirred mixture of 2,3-dihydroindole-2-carboxylic acid ethyl ester (4.78 g., 25.0 mmole), triethylamine (2.7 g., 26.7 mmole), and anhydrous ether (500 ml) was added dropwise methacryloyl chloride (2.9 g., 27.7 mmole) dissolved in a small amount of ether. After the completion of the addition, the ice bath was removed, and the reaction mixture was stirred for 4 hours. The precipitate which separated was removed by filtration, and the filter residue was washed with ether. The combined filtrate and washing were washed with water (two 700-ml portions), then with saline, and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure on a rotary evaporator gave the prouct as an oil. The product was purified by preparative HPLC (Prep LC/System 500, Waters Associates), using a micro porasil column eluted with a mixture of hexane (95%) and ethyl acetate (5%). The crude oil may be used directly in the following reaction
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04396773 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-0504f55b11d54e99a751adb8ac487f36 |
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| Source note | uspto-grants-1983_08 |
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