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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399309Generated: October 31, 2026

Water → 6-iodo-2,2,3-trimethyl-1(2H)-benzopyran

https://huagongshe.com/reaction/2399309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantSodiumHCID 5360545—
Reactant2-(1-Methyl-2-oxo-propyloxy)-5-iodobenzyltriphenylphosphonium bromideHCID 86748955—
SolventEthanolHCID 702—
Product6-iodo-2,2,3-trimethyl-1(2H)-benzopyranHCID 1938688785%

Reaction Steps

To a suspension of 2-(1-methyl-2-oxo-propyloxy)-5-iodobenzyltriphenylphosphonium bromide (0.71 g, 0.00108 mol) in absolute ethanol (3 ml) was added dropwise at room temperature a solution of sodium (0.025 g) in absolute ethanol (1 ml). After twelve hours at room temperature, diethyl ether and water were added. The organic phase was separated, dried and evaporated. The residue was chromatographed on silica gel, eluting with a mixture of dichloromethane/heptane (50/50) to give 0.29 g (85%) of 6-iodo-2,2,3-trimethyl-1(2H)-benzopyran, as an oil, 1NMR (CDCl3): δ1.4 (s, 6H), 1.8 (s, 3H), 6.0 (s, 1H), 6.55 (d, 1H), 7.2 (d, 1H), 7.35 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05447943
Source datasetuspto-grants-1995_09
ORD IDord-d9b897b047a54d7f83d91b92ba28da52
Source noteuspto-grants-1995_09