تفاعل #3788

ord-206a6fa334884220975b99cf576fbf83

معادلة التفاعل

CON(C)C(=O)c1ccccc1
N-methoxy-N-methylbenzamide
Cl
HCl
CN(C)CCN(C)C
N,N,N',N'-tetramethylethylene diamine
Sc1ccccc1
thiophenol
[Li][CH2]CCC
n-butyllithium
O=C(c1ccccc1)c1ccccc1S
title compound
المردود 59.6%
O=C(c1ccccc1)c1ccccc1S
2-Mercaptobenzophenone
المردود 59.6%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGAfter stirring for 20 minutes
  2. 2
    أخرىThe product was partitioned between ethyl acetate
  3. 3
    أخرىThe layers were separated
  4. 4
    غسيلthe organic portion was washed with brine
  5. 5
    تجفيفdried (Na2SO4)
  6. 6
    ترشيحfiltered
  7. 7
    تركيزthe filtrate was concentrated in vacuo
  8. 8
    أخرىThe liquid obtained
  9. 9
    أخرىwas purified

الإجراء التجريبي

To a solution of N,N,N',N'-tetramethylethylene diamine (4.4 g, 0.038 mol) and thiophenol (2 g, 0.018 mol) in cyclohexane (40 mL) was added dropwise n-butyllithium (24 mL, 0.038 mol) at room temperature. The suspension was stirred under nitrogen for 16 hours, followed by the dropwise addition of N-methoxy-N-methylbenzamide (3.39, 0.019 mol). After stirring for 20 minutes, the reaction mixture was added to cold aqueous HCl (1N). The product was partitioned between ethyl acetate and the acidic solution. The layers were separated and the organic portion was washed with brine, dried (Na2SO4), filtered, and the filtrate was concentrated in vacuo. The liquid obtained was purified using silica gel chromatography (75% hexane/25% ethyl acetate) to give 2.3 g of the title compound as a viscous yellow liquid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05734081uspto-grants-1998_03