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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715636Generated: November 2, 2026

Sodium Iodide → Methyl (S)-2-(Boc-amino)-4-iodobutanoate

https://huagongshe.com/reaction/1715636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethyl (S)-2-(Boc-amino)-4-bromobutyrateHCID 10685328—
SolventAcetoneHCID 180—
ProductMethyl (S)-2-(Boc-amino)-4-iodobutanoateHCID 1439415092%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799782B2
Source datasetuspto-grants-2010_09
ORD IDord-72608d66019440e6900203f19c2d1e8c
Source noteuspto-grants-2010_09