Sodium Carbonate → HCID 57224461, compound

HRID 843435Notes

Reaction equation

HRID 843435 reaction equation
O[C@@H](C1C=CC=CC=1)C([O:5][C@@H:6]1[C@@H:11]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[C@H:10]([CH2:20][O:21][C:22]([C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:9][N:8]([CH2:41][C:42]2[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=2)[CH2:7]1)=O.C(=O)([O-])[O-].[Na+].[Na+]>O.C(OCC)(=O)C>[CH2:41]([N:8]1[CH2:9][C@@H:10]([CH2:20][O:21][C:22]([C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=2)([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C@H:11]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)[C@@H:6]([OH:5])[CH2:7]1)[C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1

Participants

5

Procedure

33.3 (46.13 mmol) of (3R,4R,5S)-1-benzyl-4-(4-methoxy-phenyl)-5-trityloxymethyl-piperidin-3-ol (S)-hydroxy-phenyl-acetate were treated with a cold aqueous solution of 7.3 g (69.2 mmol) of sodium carbonate in 100 ml water and 600 ml of ethyl acetate. The aqueous phase was separated and extracted twice with 200 ml of ethyl acetate. The combined organic phases were dried over sodium sulfate and evaporated under reduced pressure to yield 25 g of (3R,4R,5S)-1-benzyl-4-(4-methoxy-phenyl)-5-trityloxymethyl-piperidin-3-ol as a colorless oil which was directly used without further purification.

Workup

  1. customThe aqueous phase was separated
  2. extractionextracted twice with 200 ml of ethyl acetate
  3. dry with materialThe combined organic phases were dried over sodium sulfate
  4. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-b7f14f7701ba41edb3609ddeb2198ee7
Source dataset
uspto-grants-2002_04
Patent number
US06376672B1

Reaction notes

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