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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383370Generated: October 29, 2026

Iodoethane → Ethyl (2-chloro-5-(boc-amino)phenyl)acetate

https://huagongshe.com/reaction/1383370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(5-{[(Tert-butoxy)carbonyl]amino}-2-chlorophenyl)acetic acidHCID 22600094—
SolventAcetoneHCID 180—
ProductEthyl (2-chloro-5-(boc-amino)phenyl)acetateHCID 5392230398%

Reaction Steps

To a solution of (2-chloro-5-(Boc-amino)phenyl)acetic acid (2.8 g; 9.8 mmol; from step (iv) above) in acetone (100 mL) was added K2CO3 (2.1 g, 15 mmol). EtI (70.6 g; 150 mmol) was then added whilst the reaction mixture was stirred and refluxed. The solution was concentrated, and the resultant mixture was partitioned between ether and water (1:1; 60 mL). The organic layer was separated, and the water layer was extracted once with ether (30 mL). The combined organic phase was washed with water, dried (Na2SO4), and concentrated to yield 3.0 g (98%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255301B1
Source datasetuspto-grants-2001_07
ORD IDord-a9b4b63a9f1e40e4bfbbb50196559c09
Source noteuspto-grants-2001_07