HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863Generated: October 23, 2026
Triethylamine → [1-(N-phenylmethoxycarbonylcarbamimidoyl)pyrrolidin-3-yl]methyl methanesulfonate
https://huagongshe.com/en/reaction/863
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | benzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamate | HCID 140379085 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | [1-(N-phenylmethoxycarbonylcarbamimidoyl)pyrrolidin-3-yl]methyl methanesulfonate | HCID 140379087 | 50% |
Reaction Steps
0.7 g (2.53 mmole) (3RS)-1-(N-benzyloxycarbonylamidino)-3-hydroxymethyl pyrrolidine and 0.70 ml (5.05 mmole) triethylamine was dissolved in 15 ml diethyl ether/CH2Cl2 1/1 and the mixture was cooled to 0° C. 0.25 ml (3.29 mmole) methanesulphonyl chloride in 3 ml diethyl ether was slowly added and the reaction mixture was stirred at 0° C for three hours. The solvent was evaporated and the residue was dissolved in ethyl acetate and extracted with a 0.3M KHSO4 -solution. The water layer was washed once with CH2Cl2. The water layer was made neutral with 10M NaOH-solution and extracted twice with CH2Cl2. The combined organic layer was dried (Na2 SO4), filtered and evaporated to yield 0.450 g (50%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723444 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-50d2591cf07947e7ab725904f4df96f4 |
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| Source note | uspto-grants-1998_03 |
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