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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367192Generated: October 30, 2026

Methyl iodide → HCID 66973304, compound

https://huagongshe.com/reaction/1367192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 66865136HCID 66865136—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66973304HCID 66973304—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 1 M solution of sodium bis(trimethylsilyl)amide in THF (0.642 mL, 0.642 mmol) at −78° C. was added dropwise a solution of tert-butyl (2S)-2-(3,5-difluorophenyl)-6-oxopiperidine-1-carboxylate (200 mg, 0.642 mmol, described in Intermediate 26) in DME (10 mL) at −78° C. The resulting mixture was stirred at −78° C. for 10 min then iodomethane (0.040 mL, 0.642 mmol) was added. After stirring at −78° C. for 30 min and at −30° C. for 30 min, the reaction mixture was cooled to −78° C. and quenched with saturated aqueous NH4Cl (10 mL) and extracted with EtOAc (2×10 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 90:10. MS: m/z=270 (M−C4H7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893079B2
Source datasetuspto-grants-2011_02
ORD IDord-f6b35ce8b71f4019b4cb31e02b72ea8e
Source noteuspto-grants-2011_02