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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455343Generated: November 2, 2026

Methyl iodide → HCID 21075141, compound

https://huagongshe.com/reaction/1455343

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 numberUS07482335B2
Source datasetuspto-grants-2009_01
ORD IDord-2a8fee93c8c64430aee58b53f85d41c7
Source noteuspto-grants-2009_01