Boron trifluoride etherate → HCID 68469064, compound

HRID 7676Notes

Reaction equation

HRID 7676 reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([S:11][CH3:12])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[Li]CCCC.B(F)(F)F.CCOCC.[O:27]1[CH:33]2[CH:28]1[CH2:29][O:30][CH2:31][CH2:32]2.[NH4+].[Cl-]>C1COCC1.CCOC(C)=O>[CH3:12][S:11][C:8]1[CH:9]=[CH:10][C:5]([S:2]([CH2:1][C@@H:33]2[CH2:32][CH2:31][O:30][CH2:29][C@H:28]2[OH:27])(=[O:4])=[O:3])=[CH:6][CH:7]=1

Participants

8

Conditions

Temperature
-78 °C

Procedure

1-Methanesulfonyl-4-methylsulfanyl-benzene (4.33 g) was dissolved in THF (50 mL) and cooled to −78° C. prior to the addition of 1.6 M nBuLi (13.4 mL). After 0.5 h, BF3-Et2O (2.7 mL) was added followed (±)3,4-epoxytetrahydropyran (1.2 g) (Tetrahedron 1974, 4013). After an addition 1 h at −78° C., the solution was warmed to 0° C. After 2 h, the solution was cooled to −78° C. and saturated NH4Cl solution (aq) was added. The solution was warmed to rt and EtOAc was added. The organic layer was washed with brine, dried, filtered, and concentrated. Flash chromatography of the resulting residue gave (±)(3S*,4R*)-4-(4-methylsulfanyl-benzenesulfonylmethyl)-tetrahydro-pyran-3-ol (1.3 g) as the major product. MS found: (M+H)+=303.0.

Workup

  1. additionAfter an addition 1 h at −78° C.
  2. temperaturethe solution was warmed to 0° C
  3. waitAfter 2 h
  4. temperaturethe solution was cooled to −78° C.
  5. temperatureThe solution was warmed to rt
  6. washThe organic layer was washed with brine
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-8e6cc379dfa349a28ee987c02c5121ab
Source dataset
uspto-grants-2006_08
Patent number
US07087604B2

Reaction notes

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