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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070133Generated: October 30, 2026

Methyl iodide → HCID 13821420, compound

https://huagongshe.com/reaction/2070133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN-((tert-Butoxy)carbonyl)-D-tryptophanHCID 111050—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 13821420HCID 13821420—

Reaction Steps

N-tert-Butoxycarbonyl-D-tryptophan (3.0 g) was dissolved in N,N-dimethylformaldehyde (30 mL) under argon, and potassium tert-butoxide (as 12% tetrahydrofuran solution) (17.7 g) was added dropwise thereto under cooling on ice, followed by stirring for 15 minutes. A solution of iodomethane (2.1 g) in N,N-dimethylformaldehyde (3.0 mL) was added to the mixture, and stirring was performed for 10 minutes. The resultant mixture was partitioned between 30% aqueous citric acid solution and ethyl acetate, and the organic layer was sequentially washed with 30% aqueous citric acid solution and saturated aqueous sodium chloride solution, followed by drying over sodium sulfate. The solvent was evaporated under reduced pressure, and diisopropyl ether was added to the thus-recovered residue. The precipitates were recovered through filtration, washed with diisopropyl ether, and dried under reduced pressure, whereby the title compound (1.89 g) was yielded.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299255B2
Source datasetuspto-grants-2012_10
ORD IDord-be8261d95efd469fb4697f46b6367b07
Source noteuspto-grants-2012_10