تفاعل #319066

ord-a2ebce2b9ce046349ce522148bdf6ab2

معادلة التفاعل

CCO[PH](=O)CCCCc1ccccc1
(4-phenylbutyl)-phosphinic acid, ethyl ester
C[Si](C)(C)Cl
trimethylsilyl chloride
CCN(CC)CC
triethylamine
C=CC(=O)[O-]
acrylate
CCN(CC)CC
triethylamine
CCOP(=O)(/C=C/C(=O)OC)CCCCc1ccccc1
title compound
CCOP(=O)(/C=C/C(=O)OC)CCCCc1ccccc1
(E)-3-[Ethoxy(4-phenylbutyl)phosphinyl]-2-propenoic acid, methyl ester

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزafter which it was concentrated in vacuo
  2. 2
    workup.STIRRINGThe resulting yellow mixture was stirred overnight at 65° C.
  3. 3
    أخرىresulting in an orange semisolid
  4. 4
    غسيلwashed sequentially with 1N hydrochloric acid and saturated sodium bicarbonate solution
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    تركيزconcentrated to an orange oil
  7. 7
    غسيلeluting with a gradient from 1:1 hexane

الإجراء التجريبي

A solution of (4-phenylbutyl)-phosphinic acid, ethyl ester (8.0 g, 35.4 mmols) in chloroform (40 ml) were added trimethylsilyl chloride (13.5 ml, 106 mmols) and triethylamine (19.7 ml, 142 mmols). The resulting mixture was stirred at 25° C. for 2.5 hours, after which it was concentrated in vacuo. To the residue were added methyl α-chloro=acrylate (20 g, 0.16 mole, prepared as described by C. S. Marvel and J. C. Cowan, J. Amer. Chem. Soc. 61, 3156 (1939)) and triethylamine (9.0 ml, 64 mmol). The resulting yellow mixture was stirred overnight at 65° C., resulting in an orange semisolid. The mixture was diluted with ethyl acetate and washed sequentially with 1N hydrochloric acid and saturated sodium bicarbonate solution, dried (MgSO4), and concentrated to an orange oil. The oil was chromotographed on LPS-1 silica gel, eluting with a gradient from 1:1 hexane:ethyl acetate to ethyl acetate, to give the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04849525uspto-grants-1989_07