HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844866Generated: November 1, 2026
Formaldehyde → (R)-tert-Butyl 1-methylpyrrolidin-3-ylcarbamate
https://huagongshe.com/reaction/1844866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | (3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidine | HCID 1514397 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-tert-Butyl 1-methylpyrrolidin-3-ylcarbamate | HCID 45091942 | 59.4% |
Reaction Steps
In a dried reaction flask, (R)-tert-butyl pyrrolidin-3-ylcarbamate (5.774 g, 31.0 mmol) and formaldehyde solution (37%, 6.82 mL) were dissolved into methanol (124 mL) under a nitrogen protection. The mixture was stirred at room temperature for 1 hr. Sodium borohydride (3.518 g, 93.0 mmol) was added in portion under an ice bath. The mixture was stirred at room temperature for 3 hr. Water was added and the solution was concentrated under reduced pressure. Ethyl acetate and saturated aqueous sodium bicarbonate solution were added. The mixture was extracted with ethyl acetate. The combined organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered, purified by silica gel column chromatography (ethyl acetate:petroleum ether=1:1) to produce a white solid (3.685 g) in 59.4% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946279B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-9339ebcb5d9c43e58680193ea60ff4a9 |
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| Source note | uspto-grants-2015_02 |
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