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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849424Generated: October 31, 2026

1,1-Dichloroethane → HCID 178473725, compound

https://huagongshe.com/reaction/849424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178478619HCID 178478619—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 178473725HCID 17847372548%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of Compound B (140 mg, 0.35 mmol), 4-formyl imidazole (68 mg, 0.7 mmol), dichloroethane (2 mL) and acetic acid (2 mL) was stirred at room temperature for 30 min and sodium triacetoxyborohydride (150 mg, 0.7 mmol) was added. The solution was heated to 60° C., stirred for 18 hour, and additional portions of 4-formyl imidazole and sodium triacetoxyborohydride were added (0.2 mmol each, 4 portions over 8 hours); the mixture was diluted with ethyl acetate (20 mL) and ammonium hydroxide (5 ml, conc), and stirred for an additional 30 min. The mixture was extracted with ethyl acetate (2×25 mL) and the combined organic extracts were washed with aqueous sodium bicarbonate (25 ml, saturated solution), and then ammonium chloride (25 mL, sat aqueous solution), dried (Na2SO4), and concentrated in vacuo to a semi-solid. The crude was purified by preparative HPLC (aqueous methanol gradient containing 0.1% TFA, C-18 column) and lyophilized to provide Compound C as a white solid (80 mg, 48%). MS: (M+H)+ 471

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011029
Source datasetuspto-grants-2000_01
ORD IDord-43be0825aa844e8db0ad28ca6da308b4
Source noteuspto-grants-2000_01