تفاعل #487535

ord-82544e20936a497e90e496fc7c700a7c

معادلة التفاعل

OCc1ccc(NCCCCCc2ccccc2)c(Br)c1
(3-bromo-4-((5-phenylpentyl)amino)phenyl)methanol
[O]=[Cr](=[O])([O-])[Cl].c1cc[nH+]cc1
PCC
O=Cc1ccc(NCCCCCc2ccccc2)c(Br)c1
3-bromo-4-((5-phenylpentyl)amino)benzaldehyde

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was concentrated
  2. 2
    أخرىpurified by chromatography on silica gel (ethyl acetate-hexane)

الإجراء التجريبي

A solution of 5-bromopentylbenzene [14469-83-1](4 g, 17.6 mmol) in HMPA (55 g) was treated with 4-amino-3-bromobenzemethanol [146019-46-7] and dry K2CO3 (4.87 g, 35.2 mmol) for ˜18 h at 120° C. The mixture was cooled to rt, poured onto water (600 mL) and extracted with ethyl acetate (200 mL). The organic phase was washed with water (200 mL), dried over Na2SO4, concentrated, and purified by chromatography (ethyl acetate/hexane) to give (3-bromo-4-((5-phenylpentyl)amino)phenyl)methanol (2.24 g, 37%). A solution of (3-bromo-4-((5-phenylpentyl)amino)phenyl)methanol (8.0 g, 23 mmol) in dichloromethane (160 mL) was treated with silica gel (24 g) and PCC (14.9 g, 69 mmol) at rt for ˜18 h. The mixture was concentrated, and purified by chromatography on silica gel (ethyl acetate-hexane) to give 3-bromo-4-((5-phenylpentyl)amino)benzaldehyde Intermediate-21 (3.5 g, 44%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08741875B2uspto-grants-2014_06