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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59672Generated: October 29, 2026

Bromoform → HCID 131737063, compound

https://huagongshe.com/reaction/59672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 89704989HCID 89704989—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 131737063HCID 131737063—

Reaction Conditions

Temperature60 °C

Reaction Steps

Aqueous sodium hydroxide solution (50% w/v, 1.63 mL) was added slowly to a vigorously stirred mixture of methyl 7-methoxymethyl-2H-chromene-8-carboxylate (Intermediate 9, 0.875 g), benzyltriethylammonium chloride (0.173 g) and bromoform (15 mL). The resultant mixture was vigorously stirred and heated at 60° C. for 3 hours. After cooling, the mixture was poured into a mixture of brine and ethyl acetate. The aqueous layer was further extracted with ethyl acetate and the combined organic layers were dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of TBME and cyclohexane with a gradient of 0-35% to give methyl cis-(1aRS,7bSR)-1,1-dibromo-5-methoxymethyl-1,1a,2,7b-tetrahydrocyclopropa[c]chromene-4-carboxylate (1.06 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440943B2
Source datasetuspto-grants-2016_09
ORD IDord-af975f829a5442ab94932d2b4b8ddf42
Source noteuspto-grants-2016_09