HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069801Generated: October 26, 2026
Hydrochloric Acid → (+/-)-1-BOC-amino-2-cyclopentene-4-carboxylic Acid
https://huagongshe.com/reaction/1069801
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tert-butyloxycarbonyl fluoride | HCID 9898818 | — |
| Reactant | 4-Aminocyclopent-2-ene-1-carboxylic acid hydrochloride | HCID 10171261 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (+/-)-1-BOC-amino-2-cyclopentene-4-carboxylic Acid | HCID 77801814 | 63% |
Reaction Steps
16.4 g of crude (±)-1-amino-2-cyclopentene-4-carboxylic acid hydrochloride (prepared as in J. Org. Chem. 1981, 46, 3268) were dissolved in a mixture of 80 ml of water and 80 ml of dioxane at room temperature under nitrogen. The mixture was then adjusted to pH 14 with 1 N NaOH, and a diethyl ether solution of tert-butyloxycarbonyl fluoride (BOC-F, 20% excess) was added (BOC-F prepared as in Synthesis 1975, 599). .The mixture was stirred for a further 5 h at room temperature. 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 3 times with 100 ml of ethyl acetate. The organic phase was evaporated to 50 ml and diluted with 25 ml of toluene. After cooling (0-10° C.), the title compound was filtered and dried. 14.3 g of product were obtained. The yield was 63%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06252112B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-90c56467cfce4aaa978fa30dcbec2db8 |
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| Source note | uspto-grants-2001_06 |
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