Boron trifluoride etherate → HCID 10884116, compound

HRID 552011Notes

Reaction equation

HRID 552011 reaction equation
CS(O[C@H:6]1[CH2:30][CH2:29][C@@:28]2([CH3:31])[C:8](=[CH:9][CH2:10][C@@H:11]3[C@@H:27]2[CH2:26][CH2:25][C@@:24]2([CH3:32])[C@H:12]3[CH2:13][CH2:14][C@@H:15]2[C@H:16]([CH3:23])[CH2:17][CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[CH2:7]1)(=O)=O.[Si]([N:37]=[N+:38]=[N-:39])(C)(C)C.B(F)(F)F.CCOCC.C([O-])(O)=O.[Na+]>C(Cl)Cl>[N:37]([C@H:6]1[CH2:30][CH2:29][C@@:28]2([CH3:31])[C:8](=[CH:9][CH2:10][C@@H:11]3[C@@H:27]2[CH2:26][CH2:25][C@@:24]2([CH3:32])[C@H:12]3[CH2:13][CH2:14][C@@H:15]2[C@H:16]([CH3:23])[CH2:17][CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[CH2:7]1)=[N+:38]=[N-:39]

Participants

6

Reactant 4

HCID 8000Boron trifluoride etherateHCID 78378AzidotrimethylsilaneHCID 102403Cholest-5-en-3-ol (3beta)-, 3-methanesulfonateHCID 516892Sodium Bicarbonate

Product 1

HCID 10884116HCID 10884116, compoundYield 94.1%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
22 °C

Procedure

To a solution of 3β-cholest-5-en-3-yl methanesulfonate (9.30 g, 20.0 mmol) in anhydrous CH2Cl2 (100 mL), TMSN3 (2.95 mL, 22.0 mmol) was added, followed by boron trifluoride etherate (5.0 mL, 40.0 mmol). The reaction was stirred at 22° C. for 2 h. When the starting material was no longer visible by TLC analysis (hexanes), the reaction was slowly poured into saturated aqueous NaHCO3 (100 mL) and vigorously stirred for 10 min. The organic layer was separated and the aqueous layer was extracted with diethyl ether (60 mL×2). The organic layers were combined, washed with deionized water (100 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure to give the crude product as light yellow solid. Flash column chromatography (hexanes) afforded the product (7.75 g, 94.1%) as white solid, mp 84-86° C.; 1H NMR (300 MHz, CDCl3) δ 5.38 (s, 1H), 3.26-3.15 (m, 1H), 2.28 (d, J=7.9 Hz, 2H), 2.05-0.85 (m, 38H), 0.68 (s, 3H); 13C NMR (75.4 MHz, CDCl3) δ 139.8, 122.5, 61.1, 56.7, 56.1, 50.1, 42.3, 39.7, 39.5, 38.1, 37.6, 36.6, 36.2, 35.8, 31.8, 31.7, 28.2, 28.0, 27.9, 24.2, 23.8, 22.8, 22.5, 21.0, 19.2, 18.7, 11.8; IR (film) ν max 2934, 2896, 2861, 2097, 1464, 1443, 1377, 1367, 1243, 1231 cm−1; APCI m/z 411.3607 (M+, C27H45N3 requires 411.3613).

Workup

  1. stirringvigorously stirred for 10 min
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted with diethyl ether (60 mL×2)
  4. washwashed with deionized water (100 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customto give the crude product as light yellow solid

Sources & evidence

ORD record
ord-57a896035df04a128e943d3ffb749ec9
Source dataset
uspto-grants-2011_05
Patent number
US07947647B2

Reaction notes

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