HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840519Generated: October 26, 2026
Hydrochloric Acid → (+/-)-1-BOC-amino-4-hydroxymethyl-2-cyclopentene
https://huagongshe.com/reaction/840519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tert-butyloxycarbonyl fluoride | HCID 9898818 | — |
| Reactant | (4-Aminocyclopent-2-en-1-yl)methanol hydrochloride | HCID 21933817 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (+/-)-1-BOC-amino-4-hydroxymethyl-2-cyclopentene | HCID 77801348 | 56% |
Reaction Steps
15 g of crude (±)-1-amino-4-hydroxymethyl-2-cyclopentene hydrochloride were dissolved in a mixture of 150 ml of water and 150 ml of dioxane at room temperature under nitrogen. The solution was adjusted to pH 14 with 1N NaOH, then a diethyl ether solution of tert-butyloxy-carbonyl fluoride (BOC-F, 20% excess) was added, and the mixture was stirred for a further 3 h at room temperature (BOC-F prepared as disclosed in Synthesis 1975, 599). The pH was adjusted to 2 with conc. HCl. After distillation of the organic solvents, 50 ml of water were added to the residue, and the mixture was extracted with 3×100 ml of ethyl acetate. The combined organic phases were completely evaporated. The residue was crystallized in a mixture of 110 ml of diisopropyl ether and 80 ml of n-hexane. 11.95 g of title compound were obtained. The yield was 56%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06368850B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-4c89284d185c4a8f89315987c3a06ec3 |
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| Source note | uspto-grants-2002_04 |
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