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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837673Generated: October 25, 2026

Methanol → (1S,2S)-6,7-Dibromo-2-methoxy-5,8-dimethyl-1,2-dihydronaphthalen-1-ol

https://huagongshe.com/reaction/1837673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,2,2-TrifluoroethanolHCID 6409—
Reactant5,6-Dibromo-4,7-dimethyl-1,4-epoxy-1,4-dihydronaphthaleneHCID 22678912—
Product(1S,2S)-6,7-Dibromo-2-methoxy-5,8-dimethyl-1,2-dihydronaphthalen-1-olHCID 5904108079%

Reaction Steps

To a flame dried round bottom flask, [Rh(COD)Cl]2 (1.5 mg, 0.0029 mmol), (R)-(S)-PPF-PtBu2 (3.2 mg, 0.0059 mmol) and 26 (195 mg, 0.59 mmol) were added followed by addition of trifluoroethanol (1.0 mL) and methanol (1.0 mL). The mixture was heated to reflux for 20 hours. The solvents were then removed in vacuo. The resulting solid was purified by flash chromatography (50% ethyl acetate in hexanes) to give 29 as a white crystalline solid (171.6 mg, 79%). The ee was determined to be 97% using HPLC analysis on a CHIRALCEL OD column, λ=486 nm. Retention times in 4% isopropanol in hexanes were 16.8 min (major) and 19.3 min. Rf=0.39 on silica gel (50% ethyl acetate:hexanes); mp 114-116° (Et2O); [α]25D=−197.1° (c=10.0, CHCl3); IR (KBr, cm−1) 3349(s), 2901 (m), 1700(w), 1532 (w), 1404(m), 1258 (m), 1081 (s), 936 (s); 1H NMR (400 MHz, CDCl3) δ 6.96-6.93 (1H, m), 6.23-6.19 (1H, m), 4.89 (1H, s), 3.96-3.90 (1H, m), 3.38-3.35 (3H, m), 2.61-2.57 (3H, m), 2.54 (3H, s), 1.82-1.54 (1H, m); 13C NMR (400 MHz, CDCl3) δ 137.3, 134.4, 133.2, 129.7, 129.5, 129.0, 128.1, 125.3, 75.3, 66.6, 56.6, 21.0, 20.6. HRMS calcd for C13H16O2Br2 (M+): 361.9518. Found: 361.9335.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784210B2
Source datasetuspto-grants-2004_08
ORD IDord-75f299e6443942eb8c17881fb260b657
Source noteuspto-grants-2004_08