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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225156Generated: November 1, 2026

Methyl iodide → HCID 21075141, compound

https://huagongshe.com/reaction/2225156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 21075142HCID 21075142—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21075141HCID 21075141298.2%

Reaction Steps

Preparation C6, Step 1. Ethyl 3-(adamant-1-yl)-pyrrole-5-carboxylate (0.20 g, 0.7 mmol, 1 eq) was dissolved in THF (20 mL). Potassium bis(trimethylsilyl)amide (0.5 M in Tol, 1.62 mL, 0.81 mmol, 1.1 eq) was added thereto followed by iodomethane (.0.102 mL, 1.6 mmol, 2.2 eq). The next day, the same amounts of potassium bis(trimethylsilyl)amide and iodomethane were again added to drive the reaction to completion. In 4 h, the reaction was finished. Ethyl acetate was added (100 mL) and the organic layer was washed with water (2×), brine, dried (MgSO4) and stripped to yield 600 mg of ethyl 3-(adamant-1-yl)-1-methylpyrrole-5-carboxylate, which was used as is in the next step. MS found: (M+H)+=288.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378409B2
Source datasetuspto-grants-2008_05
ORD IDord-0e5827da7a0b43b69dddbf70f2fa00b7
Source noteuspto-grants-2008_05