Efficient synthesis of 6-mono-bromo-1,1′-bi-2-naphthol

被引：30

作者：

Cai, DW ^{[1
]}

Larsen, RD ^{[1
]}

Reider, PJ ^{[1
]}

机构：

[1] Merck & Co Inc, Merck Sharp & Dohme Res Labs, Dept Proc Res, Rahway, NJ 07065 USA

来源：

TETRAHEDRON LETTERS | 2002年 / 43卷 / 22期

关键词：

6-mono-bromo-1,1 '-bi-2-naphthol; bromination;

D O I：

10.1016/S0040-4039(02)00730-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Through mono-ester formation of 1.1'-bi-2-naphthol (BINOL) with pivaloyl chloride the selective mono-bromination was achieved cleanly on the other ring to afford 6-mono-bromo-1,1'-bi-2-naphthol in an efficient 86% yield. (C) 2002 Elsevier Science Ltd. All rights reserved.

引用

页码：4055 / 4057

页数：3

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