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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531811Generated: November 3, 2026

Dibromomethane → HCID 21250649, compound

https://huagongshe.com/reaction/1531811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant4-IodobenzaldehydeHCID 96657—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
ReactantHCID 21250577HCID 21250577—
CatalystZincHCID 23994—
CatalystZinc SulfateHCID 24424—
SolventDimethylformamideHCID 6228—
ProductHCID 21250649HCID 21250649—

Reaction Conditions

Temperature70 °C

Reaction Steps

Zinc dust (253 mg) was stirred under nitrogen overnight. To this was added DMF (5 ml) and dibromomethane (55 mg) dissolved in DMF (1 ml) and the mixture warmed to ˜70° C. The reaction mixture was cooled to room temperature and chlorotrimethylsilane (32 mg) in DMF (1 ml) added and stirred at room temperature for 15 minutes. To this was added 2-iodo-N-Boc-azetidine (Billotte, S., Synlett, 1998, 379-380) (1.04 g) in DMF (5 ml). The reaction mixture warmed to 40° C. and the mixture sonicated for 30 minutes during which time the zinc powder dissolved to leave a hazy solution. To the solution of zincate was added 4-iodobenzaldehyde (Preparation 43) (851 mg in 5 ml DMF), tri-2-furylphosphine (35 mg in 1 ml DMF) and Pd(dbq)2 (42 ml in 1 ml DMF). The resulting mixture was heated at 60-70° C. for 4 hours, cooled to room temperature and partitioned between ammonium chloride solution and diethyl ether, and the aqueous layer was extracted with diethyl ether (3×). The combined organic extracts were dried (Na2SO4), evaporated in vacuo and purified over silica (pentane:ethyl acetate; 4:1) to afford the title compound as a mobile oil, 626 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200978B1
Source datasetuspto-grants-2001_03
ORD IDord-323e4c0949d04e15b5122a2b3f798784
Source noteuspto-grants-2001_03