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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070888Generated: November 3, 2026

Water → HCID 22398278, compound

https://huagongshe.com/reaction/1070888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22398226HCID 22398226—
SolventMethanolHCID 887—
ProductHCID 22398278HCID 2239827889.57%

Reaction Steps

To the solution of 1-Bromo-3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthalenol (12.8 g, 43.06 mmol) and sodium methoxide in methanol (5.0M) was added CuBr (1.24 g, 8.61 mmol) followed by ethyl acetate (2.5 mL). The reaction was stirred and heated to reflux for 16 hours. The reaction mixture was cooled to room temperature then poured into water and extracted with ethyl acetate. The separated organic layer was washed with brine, dried over magnesium sulfate and concentrated to yield 1-Methoxy-3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthalenol (9.58 g, 89.57%). 1H NMR (CDCl3): δ 1.27 (s, 6H), 1.36 (s, 6H), 1.63-1.67 (m, 4H), 2.21 (s, 3H), 2.53 (s, 3H), 2.57 (s, 3H), 3.87 (s, 3H), 3.90 (s, 3H), 5.15 (d, 1H), 6.30 (s, 1H), 6.94 (s, 1H), 6.98 (s, 1H), 7.13 (d, 1H), 8.35 (s, 1H). APCI-MS m/z 532 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903132B2
Source datasetuspto-grants-2005_06
ORD IDord-432e20104e7d4dbdadb907ca71899da4
Source noteuspto-grants-2005_06