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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535026Generated: October 26, 2026

Sodium Iodide → 1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartate

https://huagongshe.com/reaction/535026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-2-chloromethyl-1-propeneHCID 15859—
Reactant1-Benzyl 4-(tert-butyl) benzyl-L-aspartateHCID 16069553—
SolventAcetonitrileHCID 6342—
Product1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartateHCID 1606955458.3%

Reaction Conditions

Temperature81 °C

Reaction Steps

Part 2: A mixture of (2S)-benzylamino-succinic acid 1-benzyl ester 4-tert-butyl ester (12.1 g, 32.6 mmol), K2CO3 (14 g, 3 equiv.), NaI (3.0 g, 20 mmol) and 3-chloro-2-chloromethyl-1-propene (5.1 g, 40.8 mmol) in MeCN (150 mL) was stirred at 81° C. for 16 h. After cooling, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Purification by Combiflash (hexane and ethyl acetate: gradient 0 to 8% during 12 min) afforded (2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester (8.7 g, 58%). MS (ESI): 458 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853243B2
Source datasetuspto-grants-2014_10
ORD IDord-14d79db453ec4684b8d84ad0efc61787
Source noteuspto-grants-2014_10