Water → HCID 14397660, compound

HRID 1088742Notes

Reaction equation

HRID 1088742 reaction equation
[CH3:1][O:2][C:3]([C:5]1[CH:15]=[CH:14][CH:13]=[CH:12][C:6]=1[CH:7]=[CH:8][C:9](O)=[O:10])=[O:4].[BH4-].[Na+].O>CCOCC>[CH3:1][O:2][C:3]([C:5]1[CH:15]=[CH:14][CH:13]=[CH:12][C:6]=1/[CH:7]=[CH:8]/[CH2:9][OH:10])=[O:4]

Participants

5

Reactant 3

HCID 962WaterHCID 4311764Sodium borohydride2×HCID 54530128HCID 54530128, compound

Product 1

HCID 14397660HCID 14397660, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

2-Methoxycarbonylcinnamic acid, m.p. 176° C., was prepared by the method described in Example 2(a) and converted to the acid chloride, m.p. 75°-80° C., by the method described in Example 2(b). A solution of this acid chloride (15.5 g) in ether (250 ml) was added to a stirred suspension of sodium borohydride on alumina (60 g - prepared by addition of a solution of 1 part of sodium borohydride in 2 parts of water to 10 parts of alumina, with cooling, followed by drying under vacuum) in ether (360 ml). The mixture was stirred for 2 hours at room temperature and filtered. The filtrate was washed with 10% sodium carbonate solution, then with saturated sodium chloride solution, dried and evaporated to yield the title compound as a colourless oil.

Workup

  1. temperaturewith cooling
  2. dry with materialby drying under vacuum) in ether (360 ml)
  3. filtrationfiltered
  4. washThe filtrate was washed with 10% sodium carbonate solution
  5. dry with materialwith saturated sodium chloride solution, dried
  6. customevaporated

Sources & evidence

ORD record
ord-a55ff0ca6c1543e084eb37ac9b945a75
Source dataset
uspto-grants-1990_10
Patent number
US04963578

Reaction notes

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