Hydrochloric Acid → 1,4'-Bipiperidin-4-ol

HRID 1070928

Reaction equation

HRID 1070928 reaction equation
C(O[C:6]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][CH2:9]1)=O)(C)(C)C.OC1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].Cl>ClC(Cl)C.CO.C(O)(=O)C>[N:8]1([CH:6]2[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]2)[CH2:9][CH2:10][CH:11]([OH:14])[CH2:12][CH2:13]1

Participants

8

Procedure

4-Oxo-piperidine-1-carboxylic acid tert-butyl ester (20 g) and 4-hydroxypiperidine (6.7 g) were stirred together in dichloroethane (200 ml) with acetic acid (4 ml) at RT for 30 minutes. Sodium triacetoxyborohydride (23 g) was then added and the mixture stirred at RT overnight. The mixture was evaporated to dryness and the residue taken into water, extracted with diethyl ether (3×200 ml), the aqueous was basified to pH 9-10 and extracted with dichloromethane (3×200 ml). The dichloromethane extracts were combined, dried (MgSO4) and evaporated to leave an oil (19 g; same compound as Example 9 step 1). The oil was dissolved in methanol (300 ml) and treated with concentrated hydrochloric acid (5 ml). The mixture was stirred overnight and then evaporated to dryness to leave the title compound as the hydrochloride salt (15 g).

Workup

  1. customThe mixture was evaporated to dryness
  2. extractionextracted with diethyl ether (3×200 ml)
  3. extractionextracted with dichloromethane (3×200 ml)
  4. dry with materialdried (MgSO4)
  5. customevaporated
  6. customto leave an oil (19 g; same compound as Example 9 step 1)
  7. stirringThe mixture was stirred overnight
  8. customevaporated to dryness

Sources & evidence

ORD record
ord-db176aec055d46a99ecf4fb9576e0545
Source dataset
uspto-grants-2005_06
Patent number
US06903115B2

Linked notes

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