Ammonium Chloride → HCID 69760958, compound

HRID 2306762Notes

Reaction equation

HRID 2306762 reaction equation
[CH2:1]([O:3][C:4](=[O:20])[C:5]1[CH:10]=[CH:9][C:8]([CH2:11]P(OCC)(OCC)=O)=[CH:7][CH:6]=1)[CH3:2].C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[CH3:31][C:32]1([CH3:50])[CH2:40][CH2:39][C:38]([CH3:42])([CH3:41])[C:37]2[CH2:36][C:35]([CH2:45][CH2:46][CH2:47][CH2:48][CH3:49])([CH:43]=O)[CH2:34][C:33]1=2.[Cl-].[NH4+]>C1COCC1.CCCCCC>[CH2:1]([O:3][C:4](=[O:20])[C:5]1[CH:6]=[CH:7][C:8](/[CH:11]=[CH:43]/[C:35]2([CH2:45][CH2:46][CH2:47][CH2:48][CH3:49])[CH2:34][C:33]3[C:32]([CH3:31])([CH3:50])[CH2:40][CH2:39][C:38]([CH3:42])([CH3:41])[C:37]=3[CH2:36]2)=[CH:9][CH:10]=1)[CH3:2]

Participants

7

Procedure

0.7 g of 4-(diethoxy-phosphorylmethyl)-benzoic acid ethyl ester were dissolved in 10 ml of THF and treated at −20° C. with 2.2 ml of a 1 molar solution of lithium bis(trimethylsilyl)amide in hexane. After 15 minutes a solution of 0.46 g of 4,4,7,7-tetramethyl-2-pentyl-2,3,4,5,6,7-hexahydro-1H-indene-2-carbaldehyde in 5 ml of THF was added. The reaction mixture was stirred for 3 hours at room temperature, poured on ice cold, saturated aqueous ammonium chloride solution, extracted with ethyl acetate, the organic phase was dried (Na2SO4) and the solvent evaporated. The yellow, oily residue was purified with flash chromatography (silica gel, hexane/10% ethyl acetate) and gave 0.73 g of (E)-4-[2-(4,4,7,7-tetramethyl-2-pentyl-2,3,4,5,6,7-hexahydro-1H-indene-2-yl)-vinyl]-benzoic acid ethyl ester as colorless oil.

Workup

  1. extractionextracted with ethyl acetate
  2. dry with materialthe organic phase was dried (Na2SO4)
  3. customthe solvent evaporated
  4. customThe yellow, oily residue was purified with flash chromatography (silica gel, hexane/10% ethyl acetate)

Sources & evidence

ORD record
ord-f18b8aebcefe481396ef89305e26db8a
Source dataset
uspto-grants-2004_12
Patent number
US06828337B2

Reaction notes

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