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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776674Generated: October 27, 2026

Methyl iodide → S-3-(tert-butoxycarbonyl(methyl)amino)propyl ethanethioate

https://huagongshe.com/reaction/1776674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantS-3-(tert-butoxycarbonylamino)propyl ethanethioateHCID 14194548—
SolventTetrahydrofuranHCID 8028—
ProductS-3-(tert-butoxycarbonyl(methyl)amino)propyl ethanethioateHCID 1419455285%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of NaH (0.57 g, 60%, 14.25 mmol) in 20 ml of THF at 0° C. was added S-3-(tert-butoxycarbonylamino)propyl ethanethioate (1.25 g, 5.36 mmol) under Ar. After stirring at 0° C. for 30 min, MeI (1.0 ml, 16.06 mmol) was added to the mixture. Stirring was continued at 0° C. for 2 h then RT overnight. The mixture was concentrated, redissolved in 120 ml of EtAc/Hexane (1:2), washed with 1 M NaH2PO4 NaCl (conc.), dried over MgSO4, filtered, evaporated and purified on SiO2 chromatography eluted with EtAc/Hexane (1:7) to afford 1.121 g (85%) of the title compound. 1H NMR (CDCl3) 3.69 (t, 2H, J=7.3 Hz), 2.41 (t, 2H, J=7.3 Hz), 2.39 (s, 3H), 2.03 (s, 3H), 1.76 (m, 2H), 1.47 (s, 9H); 13C NMR 173.21, 153.39, 83.28, 43.67, 31.84, 28.26, 28.19, 27.11, 15.65; MS m/z+270.0 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265841B2
Source datasetuspto-grants-2016_02
ORD IDord-527b8359e6d743d395098628369e678a
Source noteuspto-grants-2016_02