Acetic Acid → (3S,4R)-1-(t-butyldimethylsilyl)3-[(R)-1-hydroxyethyl]-4-[2,2,2-tri(methylthio)ethyl]azetidin-2-one

HRID 648684Notes

Reaction equation

HRID 648684 reaction equation
CCC(C)[BH-](C(C)CC)C(C)CC.[K+].[I-].[K+].[Si:17]([N:24]1[C@H:27]([CH2:28][C:29]([S:34][CH3:35])([S:32][CH3:33])[S:30][CH3:31])[C@@H:26]([C:36](=[O:38])[CH3:37])[C:25]1=[O:39])([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18].C(O)(=O)C>C(OCC)(=O)C.C(OCC)C>[Si:17]([N:24]1[C@H:27]([CH2:28][C:29]([S:34][CH3:35])([S:32][CH3:33])[S:30][CH3:31])[C@@H:26]([C@H:36]([OH:38])[CH3:37])[C:25]1=[O:39])([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18]

Participants

7

Procedure

K-Selectride® (3.64 ml of 0.5M, 1.82 mmol) is added by syringe to a mixture of potassium iodide (126 mg., 0.758 mmol) and (3S, 4R)-1-(t-butyl dimethylsilyl)-3-(1-oxoethyl)-4-[2,2,2-tri(methylthio)ethyl]azetidin-2-one (298 mg, 0758 mmol) in freshly distilled ethyl ether (8 ml) at room temperature. The resulting mixture is stirred at room temperature for 2.5 hours, then quenched by the addition of acetic acid (218 mg., 3.64 mmol). The resulting mixture is diluted with ethyl acetate (25 ml) and filtered through celite. Removal of solvents in vacuo gives an oil which is chromatographed on silica gel (ether:petroleum ether) to yield 252 mg of (3S, 4R)-1-(t-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl]-4-[2,2,2-tri(methylthio)ethyl]azetidin-2-one. N.M.R. (R isomer, CDCl3 +D2O) δ4.15(dq, 1), δ3.95(ddd, 1, J=9.5, 2.3), δ3.26(dd, 1, J=8, 2.3), δ2.37(m, 2), δ2.16(s, 9), δ1.37(d, 3, J=6, 6), δ1.0(s, 9), δ0.26(s, 6).

Workup

  1. filtrationfiltered through celite
  2. customRemoval of solvents in vacuo
  3. customgives an oil which
  4. customis chromatographed on silica gel (ether:petroleum ether)

Sources & evidence

ORD record
ord-84c67f75b772412ab143af6110aabc2f
Source dataset
uspto-grants-1988_04
Patent number
US04736025

Reaction notes

Loading…