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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376050Generated: October 30, 2026

4-Methylbenzyl chloride → HCID 53256309, compound

https://huagongshe.com/reaction/2376050

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzyl chlorideHCID 7722—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514397—
SolventDimethylformamideHCID 6228—
ProductHCID 53256309HCID 5325630975.2%

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 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 etluting 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465731B2
Source datasetuspto-grants-2008_12
ORD IDord-ef61adbb0ce5471bbe4c2e836f24aff1
Source noteuspto-grants-2008_12