Hydrochloric Acid → m-Bromocinnamic acid

HRID 1635674Notes

Reaction equation

HRID 1635674 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=O.C(O)(=O)[CH2:11][C:12]([OH:14])=[O:13].N1CCCCC1.Cl>N1C=CC=CC=1.O>[Br:1][C:2]1[CH:3]=[C:4](/[CH:5]=[CH:11]/[C:12]([OH:14])=[O:13])[CH:7]=[CH:8][CH:9]=1

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 867Malonic AcidHCID 8082PiperidineHCID 765833-Bromobenzaldehyde

Product 1

HCID 776461m-Bromocinnamic acid

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 1049PyridineSolvent

Conditions

Temperature
90 °C

Procedure

A magnetically stirred solution of 3-bromobenzaldehyde (86.5 g, 0.468 mol) and malonic acid (107 g, 1.03 mol) in pyridine (200 ml) was treated with piperidine (4.0 ml, 40.45 mmol) and heated at ˜90° C. for 90 min then under reflux for 30 min. The cooled mixture was poured onto ice (200 g) and water (300 ml) then acidified to pH=1 with conc. hydrochloric acid. Filtration afforded a white solid which was washed with water (4×200 ml), dried by suction and placed in an oven at 70° C. for 48 h until constant weight was obtained (96.02 g, 90%); νmax (nujol)/cm−1 3400-2000 (br. OH), 1684.5, 1631.5, 1587.0; δH (270 MHz) 6.45 (1H, d, 2-H, 3J2,3=16.2 Hz); 7.28 (1H, t, 5′-H, Jo=7.8 Hz); 7.48 (1-H, dt, 4′-H, Jo=7.9, Jm=1.3 Hz); 7.54 (1-H, dt, 6′-H, Jo=7.9, Jm=1.0 Hz); 7.70 (1-H, t, 2′-H, Jm=1.8 Hz); 7.71 (1H, d, 3-H, 3J3,2=15.8 Hz).

Workup

  1. temperatureunder reflux for 30 min
  2. filtrationFiltration
  3. customafforded a white solid which
  4. washwas washed with water (4×200 ml)
  5. customdried by suction
  6. customwas obtained (96.02 g, 90%)

Sources & evidence

ORD record
ord-abf06936f2fb4c0c8b121dfc91ddeb90
Source dataset
uspto-grants-2003_01
Patent number
US06509476B1

Reaction notes

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