HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938787Generated: October 31, 2026
Tetrahydrofuran → N-(2(R)-hydroxy-1(S)-indanyl)-trans-3-(4-pyridyl) acrylamide
https://huagongshe.com/reaction/1938787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 3-(4-Pyridine)acrylic acid | HCID 736782 | — |
| Product | N-(2(R)-hydroxy-1(S)-indanyl)-trans-3-(4-pyridyl) acrylamide | HCID 15389521 | — |
Reaction Steps
To a suspension of trans-3-(4-pyridyl)acrylic acid (10.0 g, 0.067 mol) in 500 mL of THF was added triethylamine (10.29 mL, 0.0738 mol) and the solution was cooled to 0° C. Trimethylacetyl chloride (8.68 mL, 0.0704 mol) was added and the reaction stirred for 0.5 h. 2(R)-hydroxy-1(S)-indane (10.0 g, 0.067 mmol) dissolved in 260 mL of THF was added via cannula. After 2 h the reaction was warmed to RT and stirred an additional 15 h. The solvent was removed in vacuo and the resulting solid was triturated with cold ethyl acetate (150 mL) and filtered. This was dried overnight under vacuum (0.5 mm of Hg) to provide 18.5 g of a white solid; mp 205°-207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05693803 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-47cbe5f895fc424bb28afc9ad37e3196 |
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| Source note | uspto-grants-1997_12 |
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