Tetrabutylammonium Fluoride → 3-[(R)-3-tetradecanoyloxytetradecanoylamino]-1-propanol

HRID 381185Notes

Reaction equation

HRID 381185 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][O:5][Si](C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.[C:23]([O:38][C@H:39]([CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH3:54])[CH2:40][C:41]([OH:43])=O)(=[O:37])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36].C(Cl)CCl.CI.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[C:23]([O:38][C@H:39]([CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH3:54])[CH2:40][C:41]([NH:1][CH2:2][CH2:3][CH2:4][OH:5])=[O:43])(=[O:37])[CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]

Participants

6

Procedure

In the same manner as described in Example 20-(1), 3-amino-1-(t-butyldiphenylsilyloxy)propane (470 mg, 1.5 mmol) was acylated with (R)-3-tetradecanoyloxytetradecanoic acid (680 mg, 1.5 mmol) in the presence of EDC·MeI (595 mg, 2.0 mmol) and then deprotected with TBAF (1.0 M in THF, 2.0 mL, 2.0 mmol) in THF (10 mL) to afford 698 mg (91%) of 3-[(R)-3-tetradecanoyloxytetradecanoylamino]-1-propanol as an off-white solid.

Sources & evidence

ORD record
ord-d12c6453765b4faabb3deded6c467900
Source dataset
uspto-grants-2001_10
Patent number
US06303347B1

Reaction notes

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