تفاعل #2879

ord-6f47bc261884491694bca9fab87d052d

معادلة التفاعل

Cl.ClCCN1CCCCC1
1-(2-chloroethyl)piperidine hydrochloride
CCOC(=O)c1ccc(O)cc1
ethyl 4-hydroxybenzoate
Cl.ClCCN1CCCCC1
1-(2-chloroethyl)piperidine monohydrochloride
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCC(C)=O
methyl ethyl ketone
Cl.ClCCN1CCCCC1
1-(2-chloroethyl)piperidine mono-hydrochloride
CCOC(=O)c1ccc(OCCN2CCCCC2)cc1
Ethyl 4-(2-Piperidinoethoxy)benzoate

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was cooled to about 55° C.
  2. 2
    درجة الحرارةThe resulting mixture was heated to 80° C
  3. 3
    أخرىwas consumed
  4. 4
    أخرىUpon complete reaction
  5. 5
    درجة الحرارةto cool to room temperature
  6. 6
    تركيزthe organic layer concentrated in vacuo at 40° C.
  7. 7
    أخرىThe resulting oil was used in the next step without further purification

الإجراء التجريبي

A mixture of ethyl 4-hydroxybenzoate (8.31 g), 1-(2-chloroethyl)piperidine monohydrochloride (10.13 g), potassium carbonate (16.59 g), and methyl ethyl ketone (60 mL) was heated to 80° C. After one hour, the mixture was cooled to about 55° C. and treated with additional 1-(2-chloroethyl)piperidine mono-hydrochloride (0.92 g). The resulting mixture was heated to 80° C. The reaction was monitored by thin layer chromatography (TLC), using silica-gel plates and ethyl acetate/acetonitrile/triethylamine (10:6:1, v/v). Additional portions of 1-(2-chloroethyl)piperidine hydrochloride were added until the starting 4-hydroxybenzoate ester was consumed. Upon complete reaction, the reaction mixture was treated with water (60 mL) and allowed to cool to room temperature. The aqueous layer was discarded and the organic layer concentrated in vacuo at 40° C. and 40 mm Hg. The resulting oil was used in the next step without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05731327uspto-grants-1998_03