HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451662Generated: October 26, 2026
Red-Al → (R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/451662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Red-Al | HCID 16684438 | — |
| Reactant | (R)-tert-butyl 3-((R)-(2-amino-2-oxoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate | HCID 59598485 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate | HCID 59598469 | 109.5% |
Reaction Steps
(R)-tert-butyl 3-((R)-(2-amino-2-oxoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate (1.10 g, 2.60 mmol) was dissolved in anhydrous toluene (30 mL) and cooled to 0° C. Red-Al (65% in toluene, 2.6 mL, 8.64 mmol) was added dropwise. After the addition, the reaction was stirred at rt for 12 h and quenched by adding water slowly. The resulting mixture was filtered through Celite and washing with THF. The filtrate was evaporated under reduced pressure to give crude product 1.05 g. It was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487108B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ba36621c921544d6a72ece6accfa3f07 |
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| Source note | uspto-grants-2013_07 |
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