HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641934Generated: October 30, 2026
Benzyl chloroformate → Benzyl 3-hydroxypyrrolidine-1-carboxylate
https://huagongshe.com/reaction/641934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Hydroxypyrrolidine hydrochloride | HCID 2769408 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 3-hydroxypyrrolidine-1-carboxylate | HCID 560953 | — |
Reaction Steps
Into a 500 mL 3-necked round bottom flask was placed a solution of pyrrolidin-3-ol hydrochloride (20.2 g, 163.43 mmol) in H2O (60 mL) while cooling to 5° C. Adjustment of the pH to 7 was accomplished by the NaOH (10%). This was followed by the addition of a solution of benzyl chloroformate (36.8 g, 216.47 mmol), which was added dropwise with stirring, while cooling to a temperature of 5° C. The resulting solution was allowed to react, with stirring, for 2 hours at 5° C. Then the resulting solution was allowed to react, with stirring, for 1 hour while the temperature was maintained at room temperature. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:2). The resulting solution was extracted three times with 100 mL of ethyl acetate and the organic layers combined and dried over MgSO4 and concentrated by evaporation under vacuum using a rotary evaporator. This resulted in 30 g (crude) of benzyl 3-hydroxypyrrolidine-1-carboxylate as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696229B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-256577cbe76e4983870b751478f4f7e8 |
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| Source note | uspto-grants-2010_04 |
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