Dichloromethane → HCID 58909473, compound

HRID 1296088Notes

Reaction equation

HRID 1296088 reaction equation
I[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][CH2:7][CH2:6][CH:5]2[OH:12].C(Cl)Cl.[CH2:16]([Mg]Br)[C:17]([CH3:20])([CH3:19])[CH3:18]>C1COCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH2:16]([C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][CH2:7][CH2:6][CH:5]2[OH:12])[C:17]([CH3:20])([CH3:19])[CH3:18]

Participants

6

Reactant 3

HCID 6344DichloromethaneHCID 15325881HCID 15325881, compoundHCID 178445863HCID 178445863, compound

Product 1

HCID 58909473HCID 58909473, compoundYield 46%

Reagents, catalysts & solvents 2

HCID 178418228Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)CatalystHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 6-iodochroman-4-ol (1.0 g, 3.6 mmol) in 18 ml of THF, at 0° C., was added the Pd(dppf)Cl2.CH2Cl2 (0.15 g, 0.18 mmol), followed by neopentylmagnesium bromide (10.8 ml, 10.8 mmol, 1.0 M in Et2O). The cold bath was maintained for 10 min., then removed and stirring continued overnight. The mixture was quenched with NH4Cl (30 ml) and extracted with EtOAc (3×50 ml). The combined organic layers were dried over MgSO4 and concentrated in vacuo to yield a brown oil. The crude oil was absorbed onto silica gel followed by flash chromatography (biotage 40S) 10% EtOAc/heptanes to yield 0.36 g (46%) of 6-neopentylchroman-4-ol as a white solid. Rf=0.11. HRMS (ESI+) calcd for C14H20O2 m/z 220.1463 (M+H)+; found 220.1460.

Workup

  1. temperatureThe cold bath was maintained for 10 min.
  2. customremoved
  3. customThe mixture was quenched with NH4Cl (30 ml)
  4. extractionextracted with EtOAc (3×50 ml)
  5. dry with materialThe combined organic layers were dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customto yield a brown oil
  8. customThe crude oil was absorbed onto silica gel

Sources & evidence

ORD record
ord-166a22143c034307a28aed41464c8141
Source dataset
uspto-grants-2007_07
Patent number
US07244725B2

Reaction notes

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