1,2-Epoxybutane → HCID 12651443, compound

HRID 224248Notes

Reaction equation

HRID 224248 reaction equation
[Cl-].[Cl:2][C:3]1[C:8]([CH2:9][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[C:7]([CH3:29])[C:6]([CH3:30])=[C:5]([O:31][CH3:32])[CH:4]=1.[F:33]/[C:34](=[CH:43]\[CH:44]=[C:45](/[CH3:48])\[CH:46]=O)/[C:35](/[CH3:42])=[CH:36]/[C:37]([O:39][CH2:40][CH3:41])=[O:38].C1OC1CC>CCOCC>[Cl:2][C:3]1[C:8](/[CH:9]=[CH:48]/[C:45](/[CH3:46])=[CH:44]/[CH:43]=[C:34](\[F:33])/[C:35](/[CH3:42])=[CH:36]/[C:37]([O:39][CH2:40][CH3:41])=[O:38])=[C:7]([CH3:29])[C:6]([CH3:30])=[C:5]([O:31][CH3:32])[CH:4]=1

Participants

5

Reactant 3

HCID 78341,2-EpoxybutaneHCID 12651433HCID 12651433, compoundHCID 86736594HCID 86736594, compound

Product 1

HCID 12651443HCID 12651443, compoundYield 35%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

A mixture of 6.0 g. (12.46 mmol) of 6-chloro-4-methoxy-2,3-dimethylbenzyl triphenylphosphonium chloride and 2.71 g. of ethyl (E,Z,E)-4-fluoro-3,7-dimethyl-8-oxo-2,4,6-octatrienoate in 15 ml. of 1,2-butylene oxide was heated at 110° C. in a sealed tube for 60 hours. The resulting mixture was worked up with ether in the usual manner to give 13.53 g. of crude product. This material was chromatographed on 300 g. of silica gel. Elution with 1:4 ether-petroleum ether yielded 4.65 g. of yellow crystals. Recrystallization of this material from methylene chloride-petroleum ether afforded 1.67 g. (35% yield) of pure ethyl (E,Z,E,E)-9-(6-chloro-4-methoxy-2,3-dimethylphenyl)-4-fluoro-3,7-dimethyl-2,4,6,8-nonatetraenoate as yellow crystals, mp. 126°-128° C.

Workup

  1. additionA mixture of 6.0 g
  2. customto give 13.53 g
  3. customThis material was chromatographed on 300 g
  4. washElution with 1:4 ether-petroleum ether
  5. customyielded 4.65 g
  6. customRecrystallization of this material from methylene chloride-petroleum ether
  7. customafforded 1.67 g

Sources & evidence

ORD record
ord-9d7d037f26e74d2c8cee29480c2ac722
Source dataset
uspto-grants-1980_11
Patent number
US04231944

Reaction notes

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