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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055317Generated: November 2, 2026

Methyl iodide → HCID 22277794, compound

https://huagongshe.com/reaction/2055317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPentaneHCID 8003—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 22277833HCID 22277833—
ReactantHCID 178418306HCID 178418306—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22277794HCID 22277794—

Reaction Conditions

Temperature-70 °C

Reaction Steps

3-Bromo-5,5-dioxo-2-pivaloylaminodibenzothiophene (Example 70; 0.1 g, 0.254 mmol) was suspended in dry THF (2 ml) under argon, cooled to −70° C. and 1.7 M tert-butyllithium in pentane (0.49 ml, 0.838 mmol) was added dropwise over 5 minutes. The mixture was allowed to warm to −30° C. and the suspension slowly dissolved as the solution darkened. The mixture was then re-cooled to −70° C. and iodomethane (0.17 ml, 0.279 mmol) added and stirred for 30 minutes. Saturated ammonium acetate (5 ml) and DCM (25 ml) were added and the organic phase washed with water and dried. The mixture was evaporated in vacuo and the residue purified by preparative HPLC (Dynamax C-18 60A column eluted with 30-90% acetonitrile in water plus 0.1% trifluoroacetic acid) to give the product as a colourless solid. NMR: 9.16 (s, 1H), 8.13 (d, 1H), 7.99 (s, 1H), 7.92 (d, 1H), 7.86 (s, 1H), 7.76 (t, 1H), 7.61 (t, 1H), 2.28 (s, 3H), 1.26 (s, 9H); m/z 330.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332492B2
Source datasetuspto-grants-2008_02
ORD IDord-5d714b6ca4134f0c9eccf962c15c9294
Source noteuspto-grants-2008_02