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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081996Generated: October 31, 2026

Hydrochloric Acid → 6-Bromo-4-methoxy-5-methylthiochroman

https://huagongshe.com/reaction/1081996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Methyl-6-bromothiochroman-4-oneHCID 15278478—
SolventMethanolHCID 887—
Product6-Bromo-4-methoxy-5-methylthiochromanHCID 15278479—

Reaction Conditions

Temperature0 °C

Reaction Steps

4.4 Grams (0.017 mol) of 6-bromo-5-methylthiochroman-4-one was dissolved in 10 ml of methylene chloride and 10 ml of methanol. The solution was cooled to 0° C. with a salt water-ice bath. 0.32 Grams (0.0085 mol) of sodium borohydride was gradually added so that the temperature did not exceed 10° C. While the mixture was cooled with the ice bath, it was allowed to react for 1 hour. Then, the reaction mixture was poured into 100 ml of 5% hydrochloric acid, and extracted with methylene chloride. The methylene chloride layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. Added to the resultant oil were 20 ml of methanol and 0.3 g of concentrated sulfuric acid, and the mixture was refluxed under heat for 2 hours. The reaction mixture was allowed to cool, poured into 200 ml of water and extracted with methylene chloride. The methylene chloride layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to give 4.3 g of 6-bromo-4-methoxy-5-methylthiochroman as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587484
Source datasetuspto-grants-1996_12
ORD IDord-f987da2f149f4bc1825ab3bda0b4404a
Source noteuspto-grants-1996_12