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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

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 numberUS08518983B2
Source datasetuspto-grants-2013_08
ORD IDord-9a0fbb9f4d004c2db7ee35a934689669
Source noteuspto-grants-2013_08