HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457082Generated: October 30, 2026
HCID 11801087, compound → HCID 10554728, compound
https://huagongshe.com/reaction/1457082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11801087 | HCID 11801087 | — |
| Reactant | Red-Al | HCID 16684438 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10554728 | HCID 10554728 | — |
Reaction Steps
RED-AL®, [a 3.4M, solution of sodium bis(2-methoxyethoxy)aluminum hydride in toluene] (535 ml, 1.819 mol), dissolved in anhydrous tetrahydrofuran (400 ml) was slowly added using an addition funnel to a refluxing solution of the acylation product, (R)-3-(1H-indol-3-yl)-N-(2-methoxybenzyl)-2-(N-triphenylmethylamino)propanamide (228.6 g, 0.404 mols) produced supra, in anhydrous tetrahydrofuran (1.0 L) under a nitrogen atmosphere. The reaction mixture became a purple solution. The reaction was quenched after at least 20 hours by the slow addition of excess saturated Rochelle's salt solution (potassium sodium tartrate tetrahydrate). The organic layer was isolated, washed with brine (2×), dried over anhydrous sodium sulfate, filtered, and concentrated to an oil on a rotary evaporator. No further purification was done and the product was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05846973 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-c52b961bc9d24ff9aed20a99b5495466 |
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| Source note | uspto-grants-1998_12 |
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