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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350993Generated: October 30, 2026

Iodine → 5-Formyloxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathiole

https://huagongshe.com/reaction/2350993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(3-Hydroxypropyl)-4,6,7-trimethyl-2H-1,3-benzoxathiol-5-olHCID 127577—
SolventBenzeneHCID 241—
SolventCyclohexaneHCID 8078—
Product5-Formyloxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathioleHCID 13592061—

Reaction Steps

1.5 g of triphenylphosphine and 1.5 g of iodine were dissolved in 5 ml of dimethylformamide, and the solution was stirred for 30 minutes at room temperature, after which 0.5 g of 3-(5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiole-2-yl)propanol (prepared as described in Example 71) was added, and the reaction mixture was allowed to react for 20 hours at room temperature. The reaction mixture was then poured into water and extracted with benzene. The extract was washed with water and dried over anhydrous sodium sulfate, and the benzene was distilled off under reduced pressure. The resulting crude product was subjected to silica gel column chromatography and the final reaction products were fractionated using a 1:2 by volume mixture of cyclohexane and benzene. The desired 5-formyloxy-2-(3-iodopropyl)-4,6,7-trimethyl-1,3-benzoxathiole, melting at 91°-93° C., was obtained from the fraction first eluted. Mass spectrum (m/e): 392 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871762
Source datasetuspto-grants-1989_10
ORD IDord-fccefc5327164c8292a157b17ceaac22
Source noteuspto-grants-1989_10