HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897496Generated: October 30, 2026
Sodium Iodide → Methyl (S)-2-(Boc-amino)-4-iodobutanoate
https://huagongshe.com/reaction/1897496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl (S)-2-(Boc-amino)-4-bromobutyrate | HCID 10685328 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl (S)-2-(Boc-amino)-4-iodobutanoate | HCID 14394150 | 92% |
Reaction Steps
A mixture of (S)-4-bromo-2-tert-butoxycarbonylaminobutyric acid methyl ester (1.19 g, 4.0 mmol) (Example 120, Steps A-D) and NaI (6.0 g, 40.0 mmol) in acetone (25 mL) was heated to 70° C. for 2 hours. The mixture was then cooled to room temperature, concentrated under reduced pressure and partitioned between water (10 mL) and ether (40 mL). The layers were separated and the organic layer was washed with water (10 mL), dried over MgSO4, filtered through Celite, and concentrated under reduced pressure to afford 1.26 g of the product (92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518983B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-9a0fbb9f4d004c2db7ee35a934689669 |
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| Source note | uspto-grants-2013_08 |
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