HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45255Generated: October 28, 2026
Water → tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamate
https://huagongshe.com/reaction/45255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-butyl N-((1R,3S)-3-(hydroxymethyl)cyclopentyl)carbamate | HCID 11962831 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamate | HCID 86659749 | 75% |
Reaction Steps
To a solution of 1.4 g (6.7 mmol) of tert-butyl [(1R,3S)-3-(hydroxymethyl)cyclopentyl]carbamate in 20 mL of anhydrous THF are added portionwise under argon, at room temperature, 0.27 g (6.7 mmol) of sodium hydride at 60% in oil. After stirring for 45 minutes, the medium is cooled to 0° C. and 0.8 mL (6.7 mmol) of benzyl bromide is added. After stirring for 1 hour at room temperature, the medium is hydrolysed with 30 mL of water and extracted with 2×100 mL of EtOAc, dried over Na2SO4, concentrated under reduced pressure and then purified by chromatography on a column of silica gel, eluting with a 99/1 DCM/MeOH mixture. 1.53 g of tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamate are obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541455B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-da404e7ae40b4427b191215eb8aa30fd |
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| Source note | uspto-grants-2013_09 |
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