tert-Butyl bromoacetate → HCID 10739587, compound

HRID 263445Notes

Reaction equation

HRID 263445 reaction equation
[CH:1]([C@H:4]1[CH2:8][O:7][C:6](=[O:9])[N:5]1[C:10](=[O:20])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])([CH3:3])[CH3:2].Br[CH2:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24]>>[CH:1]([C@H:4]1[CH2:8][O:7][C:6](=[O:9])[N:5]1[C:10](=[O:20])[C@@H:11]([CH2:22][C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 79177tert-Butyl bromoacetateHCID 10755432(4S)-3-decanoyl-4-propan-2-yl-1,3-oxazolidin-2-one

Product 1

HCID 10739587HCID 10739587, compound

Procedure

Following the procedure described in Referential Example 4, but using 4-(S)-isopropyl-3-(1-oxodecyl)-2-oxazolidinone (9.85 g), prepared in Referential Example 49, and tert-butyl bromoacetate (25.4 ml) as starting materials, the desired compound (9.17 g) having a m.p. of 58°-59° C. was obtained.

Sources & evidence

ORD record
ord-79066269c56a41678ef08897c30c7702
Source dataset
uspto-grants-1997_07
Patent number
US05643908

Reaction notes

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