HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45045Generated: October 29, 2026
Diethyl Ether → tert-butyl N-{[1-(hydroxymethyl)cyclopentyl]methyl}carbamate
https://huagongshe.com/reaction/45045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 1-[(tert-butoxycarbonyl)amino]methylcyclopentanecarboxylate | HCID 57478043 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl N-{[1-(hydroxymethyl)cyclopentyl]methyl}carbamate | HCID 57478044 | 77% |
Reaction Steps
To a solution of methyl 1-[(tert-butoxycarbonyl)amino]methylcyclopentanecarboxylate (1.50 g, 5.83 mmol) in THF (25.0 mL) at −78° C. was added dropwise 1.0 M diisobutylaluminum hydride in DCM (17.5 mL). The reaction was stirred for 2 hours with slow warming to −10° C. A saturated solution of K/Na tartrate was added, followed by ether. This mixture was stirred for 30 minutes at ambient temperature and the organic layer was separated and washed with water, and brine. The organic layer was then dried over sodium sulfate, and the solvent was removed in vacuo to afford the product (1.03 g, 77%). 1H NMR (300 MHz, CDCl3): 4.90 (br s, 1H), 3.27 (s, 2H), 3.06 (d, 2H), 1.5-1.17 (m, 8H), 1.44 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541425B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-b4e6cd393cb1465fb073ff6fc3e34037 |
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| Source note | uspto-grants-2013_09 |
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