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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974090Generated: October 25, 2026

1,2-Dichloroethane → (+/-)-trans-3-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-4-[(S)-(-)-3-acetylthio-2-methylpropionyloxy]-2H-1-benzopyran

https://huagongshe.com/reaction/974090

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactanttrans-2,2-Dimethyl-3-bromo-6-cyanochroman-4-olHCID 6932483—
ReactantS-(3-Chloro-2-methyl-3-oxopropyl) (S)-ethanethioateHCID 10954137—
SolventPyridineHCID 1049—
Product(+/-)-trans-3-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-4-[(S)-(-)-3-acetylthio-2-methylpropionyloxy]-2H-1-benzopyranHCID 8674523098.4%

Reaction Steps

To a mixture of 94 g of (±)-trans-3-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-4-hydroxy-2H-1-benzopyran, 800 ml of ethylene chloride and 32.4 ml of pyridine was added 66 g of (S)-(-)-3-acetylthio-2-methylpropionyl chloride under ice-cooling over 5 minutes and stirred for 1.5 hours under room temperature. The reaction mixture was washed with diluted hydrochloric acid once and 10% aqueous sodium chloride solution twice. The organic layer was separated, dried over magnesium sulfate and concentrated under reduced pressure to give 139.8 g of (±)-trans-3-bromo-6-cyano-3,4-dihydro-2,2-dimethyl-4-[(S)-(-)-3-acetylthio-2-methylpropionyloxy]-2H-1-benzopyran as a light yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066816
Source datasetuspto-grants-1991_11
ORD IDord-d4617c5c0d9748a8aa9c46d33d43fee5
Source noteuspto-grants-1991_11