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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665945Generated: November 1, 2026

Sodium Methoxide → HCID 57508896, compound

https://huagongshe.com/reaction/1665945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 57437427HCID 57437427—
ReactantHCID 178418348HCID 178418348—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 57508896HCID 57508896—

Reaction Steps

A mixture of crude 3-bromo-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid ethyl ester (774 mg, 2.44 mmol), CuO (99 mg, 1.25 mmol) and NaOMe (540 mg, 10 mmol) in methanol (3 mL) is refluxed for 76 h. The mixture is diluted with ether (75 mL) and extracted with 1 N aq. NaOH (2×30 mL). The aq. extracts are acidified with 2 N aq. HCl (75 mL) and extracted with DCM (3×50 mL). The organic extracts are dried (Na2SO4), filtered and evaporated to provide crude 3-methoxy-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (262 mg). This material is dissolved in dry diethyl ether (10 mL) and methyllithium (0.7 mL, 1.6 N in diethyl ether) is added slowly at room temperature. After 15 min, the mixture is diluted with diethyl ether (50 mL), extracted with 1 N aq. NaOH (2×5 mL), dried (Na2SO4), filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane/EA to provide 1-(3-methoxy-5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-ethanone (44 mg) as a yellow oil; LC-MS: tR=1.03 min, [M+1]=239.30; 1H NMR (CDCl3): δ 3.96 (s, 3H), 2.98 (t, J=6.4 Hz, 2H), 2.41 (s, 3H), 2.26 (s, 2H), 1.53 (t, J=6.4 Hz, 2H), 0.95 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039644B2
Source datasetuspto-grants-2011_10
ORD IDord-5713afb241a34a78ad70311f8bcc00d0
Source noteuspto-grants-2011_10