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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716237Generated: October 30, 2026

Iodoethane → (S)-methyl 2-(tert-butoxycarbonyl(ethyl)amino)propanoate

https://huagongshe.com/reaction/716237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantBoc-L-alanine methyl esterHCID 10856577—
SolventTetrahydrofuranHCID 8028—
Product(S)-methyl 2-(tert-butoxycarbonyl(ethyl)amino)propanoateHCID 5832436539%

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-methyl 2-(tert-butoxycarbonylamino)propanoate (10.0 g, 49.2 mmol) was dissolved in THF (100 mL) and cooled to 0° C. under nitrogen. Sodium hydride (60% susp. in mineral oil, 3.00 g, 75.1 mmol) was added in portions over 2 min. The reaction mixture was stirred for 5 min at 0° C. and EtI (4.80 mL, 59.5 mmol) was added. It was allowed to warm to room temperature over the period of 1 h, stirred at room temperature overnight and at 70° C. for 7 d. The reaction mixture was cooled, filtered and concentrated in vacuo. The solid was triturated with hexanes (2×70 mL), the triturates were concentrated in vacuo and the residue was purified using flash column chromatography on silica gel (330 g SiO2, hexanes:ethyl acetate 19:1-9:1) to afford the title compounds as an oil (4.40 g, 39%). [M+H] calc'd for C11H21NO4, 232. found, 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187497B2
Source datasetuspto-grants-2015_11
ORD IDord-06df4a5dec8341fd8f1946633538ae4a
Source noteuspto-grants-2015_11