HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245684Generated: October 30, 2026
Triethylamine → 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid
https://huagongshe.com/reaction/245684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | 3-azetidinecarboxylic Acid | HCID 93192 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid | HCID 10988214 | 88.2% |
Reaction Steps
To azetidine-3-carboxylic acid (49.5 mmol, 5 g) in dioxane (150 ml), water (150 ml) and triethylamine (54.4 mmol, 7.58 ml) was added N-(benzyloxycarbonyloxy)succinimide (51.9 mmol, 12.94 g) and stirred at room temperature for half an hour. The reaction mixture was quenched with water and 30 ml of 2N hydrochloric acid and extracted three times with dichloromethane. The organic layers were combined, filtered through a phase separation filter and concentrated in vacuo. The residue was dissolved in dichloromethane and extracted three times with aqueous saturated sodium hydrogencarbonate solution. The aqueous layers were combined, acidified with 2N hydrochloric acid and extracted three times with dichloromethane. The organic layers were combined, washed with brine, filtered through a phase separation filter and concentrated in vacuo to give 1-(benzyloxycarbonyl)azetidine-3-carboxylic acid (10.27 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658794B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-53da7230223e42cdb15b9b467e6d8965 |
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| Source note | uspto-grants-2014_02 |
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