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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818053Generated: November 3, 2026

Dichloromethane → HCID 57884082, compound

https://huagongshe.com/reaction/1818053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53418337HCID 53418337—
ReactantHCID 86614807HCID 86614807—
SolventMethanolHCID 887—
ProductHCID 57884082HCID 5788408244%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a 100 mL round bottom flask equipped with a magnetic stir bar was added 6 (234 mg, 1.23 mmol), benzyltriethylammonium dichloroiodate (11, 480 mg, 1.23 mmol), sodium bicarbonate (113 mg, 1.35 mmol), CH2Cl2 (5 mL) and reagent grade methanol (2 mL). The flask was equipped with a water condenser, and the mixture was heated to 40° C. with stirring until all of compound 6 was consumed, as determined by TLC analysis. CH2Cl2 (10 mL) and 10% aqueous sodium bisulfite (10 ml) were added, the organic phase was washed with brine (1×10 mL), dried over MgSO4, filtered, concentrated and dried under high vacuum. The dry, crude product was passed through a silica gel column using straight CH2Cl2 (Rf=0.5) as eluent. The reaction provided 171 mg (44%) of 7 as a yellow solid. 1H NMR (300 MHZ, CDCl3): δ 7.58 (d, J=9 Hz, 1H), 6.00 (d, J=9 Hz, 1H), 2.67 (s, 2H), 1.40 (s, 6H). 13C NMR (75.5 MHZ, CDCl3): δ 193.9, 161.3, 149.6, 145.4, 106.9, 105.8, 78.2, 73.6, 48.8, 26.5. HRMS (EI+): calculated for C11H12INO2 [M+] m/z 316.9913, found 316.9906.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598403B2
Source datasetuspto-grants-2009_10
ORD IDord-1611cf6d8baf415eb767c61ce0e1610e
Source noteuspto-grants-2009_10