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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-2-chloromethyl-1-propene | HCID 15859 | — |
| Reactant | 1-Benzyl 4-(tert-butyl) benzyl-L-aspartate | HCID 16069553 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartate | HCID 16069554 | 58.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08853243B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-14d79db453ec4684b8d84ad0efc61787 |
|---|
| Source note | uspto-grants-2014_10 |
|---|