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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458103Generated: November 2, 2026

Methyl iodide → HCID 54317668, compound

https://huagongshe.com/reaction/1458103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCyclohexaneHCID 8078—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 54441024HCID 54441024—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54317668HCID 5431766818%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1.3M s-BuLi in cyclohexane (9.8 mL, 12.8 mmol) was added dropwise to a dry-ice/acetone cooled solution of TMEDA (0.6 mL, 3.8 mmol) in THF (10 mL), followed by the dropwise addition of a solution of the compound of Example 188 (0.75 g, 3.2 mmol) in THF (5 mL). The reaction mixture was stirred at -78° C. for 30 min, then methyl iodide (2.3 g, 16 mmol) was introduced in a single portion. This mixture was stirred for 2.5 h at -78° C., then was warmed to -30° C., diluted with water, and extracted with EtOAc (2×). The combined organic extracts were dried (MgSO4), concentrated, and purified by HPLC with 1:4 EtOAc/cyclohexane to give 146 mg of the title compound as a light yellow solid, an 18% yield. m.p. 101°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849723
Source datasetuspto-grants-1998_12
ORD IDord-60be2bcf26bb4d0e9fe7d2128fd915b3
Source noteuspto-grants-1998_12