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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83931Generated: October 30, 2026

Methyl iodide → (S)-4-(tert-butoxycarbonylamino)-5-methoxy-N,N,N-trimethyl-5-oxopentan-1-aminium iodide

https://huagongshe.com/reaction/83931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 58797552HCID 58797552—
SolventTetrahydrofuranHCID 8028—
Product(S)-4-(tert-butoxycarbonylamino)-5-methoxy-N,N,N-trimethyl-5-oxopentan-1-aminium iodideHCID 86702241—

Reaction Steps

To a solution of (S)-methyl 2-(tert-butoxycarbonylamino)-5-(dimethylamino)pentanoate (5.62 g, 20.5 mmol, 1.0 eq) in THF (40 mL), was added iodomethane (1.4 mL, 22.5 mmol, 1.1 eq). The mixture was stirred at room temperature for 1 h, until the starting material was consumed as determined by LCMS analysis. The reaction mixture was concentrated and then dried under high vacuum to provide (S)-4-(tert-butoxycarbonylamino)-5-methoxy-N,N,N-trimethyl-5-oxopentan-1-aminium iodide as a white solid, which was used in the next step without purification. MS (EI) m/z 289 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846739B2
Source datasetuspto-grants-2014_09
ORD IDord-4de7ca38eed24be592498768e2f9f8cc
Source noteuspto-grants-2014_09