4-Nitrophenol → (1S,2S)-2-(4-nitrophenoxy)-1,2,-dihydronaphthalen-1-ol

HRID 1837677Notes

Reaction equation

HRID 1837677 reaction equation
[CH2:1]1[CH2:5][O:4][CH2:3][CH2:2]1.[N+:6]([C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1)([O-:8])=[O:7].C(O[CH2:19][CH3:20])C>>[N+:6]([C:9]1[CH:14]=[CH:13][C:12]([O:15][C@H:20]2[CH:19]=[CH:5][C:1]3[C:2](=[CH:5][CH:1]=[CH:2][CH:3]=3)[C@@H:3]2[OH:4])=[CH:11][CH:10]=1)([O-:8])=[O:7]

Participants

4

Reactant 3

HCID 9804-NitrophenolHCID 3283Diethyl EtherHCID 8028Tetrahydrofuran

Product 1

HCID 9903895(1S,2S)-2-(4-nitrophenoxy)-1,2,-dihydronaphthalen-1-olYield 94%

Conditions

Temperature
80 °C

Procedure

To a flame dried round-bottomed flask, [Rh(COD)Cl]2 (1.7 mg, 0.0035 mmol), (S)-(R)-PPF-PtBu2 (3.8 mg, 0.0069 mmol) and 1 (100 mg, 0.694 mmol) were added followed by addition of THF (2.5 mL) and 4-nitrophenol (483 mg, 3.47 mmol). The mixture was heated at 80° C. for 45 minutes, then poured into diethyl ether and extracted 3 times with 10% aqueous sodium hydroxide solution. The aqueous extracts were combined and back-extracted three times with diethyl ether. The combined ether extracts were washed with brine and dried with anhydrous sodium sulfate. The solvents were removed in vacuo, yielding a solid which was purified by flash chromatography on silica gel (30% ethyl acetate in hexanes) giving a white crystalline solid 3 (184 mg, 94%). The ee was determined to be 97% by formation of Mosher's ester. Fr=0.43 on silica (30% ethyl acetate:hexanes); mp 123-125° C. (dec.); [α]25D=+169.9° (c=10.3, CHCl3); IR (KBr, cm−1) 3351 (br), 3113 (w), 3071 (w), 2884 (w), 2843 (w), 1591 (s), 1503 (s), 1342 (s), 1295 (m), 1110 (m), 896 (w); 1H NMR (400 MHz, CDCl3): δ 8.18 (2H, d, J=9.2 Hz), 7.62-7.60 (1H, m), 7.31-7.29 (2H, m), 7.15-7.13 (1H, m), 6.99 (2H, d, J=9.2 Hz), 6.57 (1H, d, J=9.9 Hz), 5.94 (1H, d, J=9.9 Hz), 5.20 (2H, s), 2.61 (1H, s); 13C NMR(400 MHz, CDCl3): δ 162.6, 141.8, 135.0, 131.5, 130.2, 128.5, 128.4, 126.8, 126.0, 125.5, 124.1, 115.4, 79.6, 72.0.

Workup

  1. extractionextracted 3 times with 10% aqueous sodium hydroxide solution
  2. extractionback-extracted three times with diethyl ether
  3. washThe combined ether extracts were washed with brine
  4. dry with materialdried with anhydrous sodium sulfate
  5. customThe solvents were removed in vacuo
  6. customyielding a solid which
  7. customwas purified by flash chromatography on silica gel (30% ethyl acetate in hexanes)

Sources & evidence

ORD record
ord-3c494e40f7d24fd485dd78ed027230a3
Source dataset
uspto-grants-2004_08
Patent number
US06784210B2

Reaction notes

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