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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899275Generated: October 25, 2026

Sodium Bicarbonate → 7-Bromo-4,4-dimethylthiochroman

https://huagongshe.com/reaction/899275

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactantm-Bromophenyl 3-methyl-2-butenyl sulfideHCID 22640690—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product7-Bromo-4,4-dimethylthiochromanHCID 2239309986.6%

Reaction Steps

A solution of 1-bromo-3-(3-methyl-but-2-enylsulfanyl)-benzene (5.651 g, 22 mmole) in 100 mL of toluene was treated with 5.433 g of p-toluenesulfonic acid monohydrate and heated at reflux for 15 hours. The mixture was diluted with 100 mL of water, neutralized with solid sodium bicarbonate and extracted with two 100 mL portions of ethyl acetate. The organic phase was dried over MgSO4, filtered and concentrated in vacuo to give a yellow oil. The product was purified by short path distillation (T=190° C. at 1.08 Torr) to give 4.902 g of 7-bromo-4,4-dimethyl-thiochroman as a pale yellow oil, which contained approximately 20% 5-bromo-4,4-dimethyl-thiochroman.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354931B2
Source datasetuspto-grants-2008_04
ORD IDord-7f5874c302d1406197f2a223c30302c2
Source noteuspto-grants-2008_04