Triethylamine → (Z,E,E)-N-ethyl-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraenamide

HRID 26980

反応式

HRID 26980 の反応式
[OH:1][CH2:2]/[C:3](/[CH2:13][CH2:14]/[CH:15]=[C:16](\[CH3:23])/[CH2:17][CH2:18][CH:19]=[C:20]([CH3:22])[CH3:21])=[CH:4]/[CH2:5][CH2:6]/[C:7](/[CH3:12])=[CH:8]\[C:9]([OH:11])=O.Cl.[CH2:25]([NH2:27])[CH3:26].C(N(CC)CC)C>CN(C)C=O>[CH2:25]([NH:27][C:9](=[O:11])/[CH:8]=[C:7](/[CH3:12])\[CH2:6][CH2:5]/[CH:4]=[C:3](/[CH2:2][OH:1])\[CH2:13][CH2:14]/[CH:15]=[C:16](\[CH3:23])/[CH2:17][CH2:18][CH:19]=[C:20]([CH3:22])[CH3:21])[CH3:26]

参加物

5

反応物 3

HCID 8471TriethylamineHCID 11198Ethylamine hydrochlorideHCID 86736493(Z,E,E)-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraenoic acid

生成物 1

HCID 86736492(Z,E,E)-N-ethyl-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraenamide

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Following the same manner as in Example 9, the reaction and after-treatment were conducted by using 1.1 g of (E,Z,E), (E,E,E), (Z,Z,E) and (Z,E,E)-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraenoic acid, 350 mg of ethylamine hydrochloride, 0.80 ml of diphenylphosphoric acid azide and 1.0 ml of triethylamine in 6.0 ml of N,N-dimethylformamide to afford 780 mg of the end product.

後処理

  1. customthe reaction

出典と根拠

ORDレコード
ord-fcc0677d475e4811b987e8238c97049a
出典データセット
uspto-grants-1979_04
特許番号
US04151357

関連ノート

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