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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013581Generated: November 1, 2026

Benzene → (6-Benzenesulfonyl-1-hydroxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-acetic acid methyl ester

https://huagongshe.com/reaction/1013581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantIodineHCID 807—
ReactantEthyl 2-bromopropionateHCID 79040—
Reactant6-benzenesulfonyl-3,4-dihydro-2H-naphthalen-1-oneHCID 59021739—
CatalystZincHCID 23994—
SolventWaterHCID 962—
Product(6-Benzenesulfonyl-1-hydroxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-acetic acid methyl esterHCID 66651224—

Reaction Steps

A solution/suspension of anhydrous benzene (25 mL), powdered Zinc metal (0.505 g, 7.72 mmol), I2 (0.01 g) and 6-benzenesulfonyl-3,4-dihydro-2H-naphthalen-1-one was stirred for 10 minutes at room temperature. Ethyl bromopropionate (0.784 mL, 1.18 g, 7.07 mmol) was added and the reaction mixture was heated to reflux for 2.5 hours. The reaction mixture was allowed to cool, diluted with 300 mL of water and extracted twice with 250 mL of EtOAc. The combined organic layers were washed with water and saturated brine, dried (MgSO4) and evaporated under reduced pressure to yield (6-benzenesulfonyl-1-hydroxy-1,2,3,4-tetrahydro-naphthalen-1-yl)-acetic acid methyl ester. MS: 375 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981923B2
Source datasetuspto-grants-2011_07
ORD IDord-e934942c50ef483a8016b488ae5bd0e3
Source noteuspto-grants-2011_07