4-hydroxy-N-(3-hydroxypropyl)benzamide → 4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol

HRID 1905521Notes

Reaction equation

HRID 1905521 reaction equation
O[CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:14])[C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1>S(Cl)(Cl)=O>[O:14]1[CH2:2][CH2:3][CH2:4][N:5]=[C:6]1[C:7]1[CH:8]=[CH:9][C:10]([OH:13])=[CH:11][CH:12]=1

Participants

3

Procedure

A mixture of 37.8 g of N-(3-hydroxypropyl)-4-hydroxybenzamide and 100 ml of thionyl chloride was stirred for 1.5 hours. The reaction mixture was concentrated in vacuo, the solid residue triturated with ethyl acetate, and converted to the free base by treatment with ammonium hydroxide. There was obtained 10.2 g of 4-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol, m.p. 196°-198° C. (from methanol).

Workup

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customthe solid residue triturated with ethyl acetate

Sources & evidence

ORD record
ord-ded16c63bd214a31b8902648d97056cc
Source dataset
uspto-grants-1989_06
Patent number
US04843087

Reaction notes

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