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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781216Generated: October 25, 2026

Mercaptoethanesulfonic acid → 1,1,4,4-Tetramethyltetralin

https://huagongshe.com/reaction/1781216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMercaptoethanesulfonic acidHCID 598—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethan-1-oneHCID 2801337—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1,1,4,4-TetramethyltetralinHCID 81186—
ProductSodiumHCID 5360545—

Reaction Steps

To a solution of 6-(bromoacetyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene (12) (15.5 mg, 0.050 mmol) in DMF (0.13 mL) and THF (0.13 mL) was added a freshly prepared solution of 2-mercapto-1-ethanesulfonic acid, sodium salt (2) (25 mg, 0.15 mmol) and potassium carbonate (21 mg, 0.15 mmol) in water (0.15 mL) at room temperature. The resulting biphasic mixture was stirred for 30 min. The reaction mixture was diluted with ethyl acetate (2.5 mL), and the organic layer was separated, washed with water (2×1 mL) and brine (1×1 mL), dried and concentrated to afford 6-[2'-mercapto-1'-ethanesulfonic acid, sodium salt)acetyl]-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene (20) as a solid. 1H NMR (pyr-d5): δ 8.19, 7.90, 7.40 (m, 3H), 4.11 (s, 2H), 3.5 (m, 4H), 1.55 (s, 4H), 1.20 (d, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05632898
Source datasetuspto-grants-1997_05
ORD IDord-bd07e98aceef4b509d4e39b6ba9624c9
Source noteuspto-grants-1997_05