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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971285Generated: October 29, 2026

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

https://huagongshe.com/reaction/971285

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 numberUS07312359B2
Source datasetuspto-grants-2007_12
ORD IDord-c57e2f6dc16f42158a6d43e2eb244af5
Source noteuspto-grants-2007_12