HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226365Generated: October 30, 2026
4-Methylbenzyl chloride → HCID 53256309, compound
https://huagongshe.com/reaction/226365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzyl chloride | HCID 7722 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidine | HCID 1514397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53256309 | HCID 53256309 | 75.2% |
Reaction Steps
To a mixture of tert-butyl (3R)-3-pyrrolidinylcarbamate (4.0 g) and 1-(chloromethyl)-4-methylbenzene (3.17 g) in DMF(40 mL) was added N-ethyl-N-isopropyl-2-propanamine (5.55 g) at ambient temperature and the resulting mixture was heated at 70° C. for four hours. The mixture was allowed to cool to ambient temperature and extracted with ethyl acetate (100 mL). The organic phase was washed with water (50 mL) and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by a flash chromatography eluting with gradient solvent system (ethyl acetate-hexane from 1:4 v/v to 1:1 v/v) to give tert-butyl [(3R)-1-(4-methylbenzyl)-3-pyrrolidinyl]carbamate (4.69 g) as a pale yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557127B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-5945a60561544ab6be9609273fa7c69e |
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| Source note | uspto-grants-2009_07 |
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