Water → p-Pentadecanoxybenzaldehyde

HRID 1863830

반응식

HRID 1863830 반응식
[OH-:1].[K+].O[C:4]1[CH:11]=[CH:10][CH:9]=[CH:8][C:5]=1[CH:6]=[O:7].Br[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27].O>CN(C)C=O.CCCCCC>[CH2:13]([O:1][C:10]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:11]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27]

참가 물질

7

반응물 4

HCID 962WaterHCID 6998SalicylaldehydeHCID 123941-BromopentadecaneHCID 14797Potassium Hydroxide

생성물 1

HCID 23127399p-Pentadecanoxybenzaldehyde

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회HCID 8058Hexane용매

실험 절차

A 100-ml four-necked flask was used, 2.79 g (42.3 mM) of 85-percent by weight caustic potash was suspended in 30 ml of dimethylformamide, and 10 ml of dimethylformamide solution containing 5.28 g (43.2 mM) of hydroxybenzaldehyde was dropped thereto while being kept at 20° C. or lower. Thereafter, aging was performed at 30° C. for 1 hour. Subsequently, 9.58 g (32.9 mM) of 1-bromopentadecane was added and aging was performed at 70° C. for 21 hours. The reaction solution was dispersed into water, and extracted with toluene. After washing with water, concentration is performed so as to produce 11.03 g of slightly colored viscous liquid. Subsequently, a recrystallization treatment was performed with hexane so as to produce 8.91 g (purity 98.3%) of p-pentadecanoxybenzaldehyde.

후처리

  1. customA 100-ml four-necked flask was used
  2. additionwas dropped
  3. customwhile being kept at 20° C.
  4. waitaging was performed at 70° C. for 21 hours
  5. extractionextracted with toluene
  6. washAfter washing with water, concentration
  7. customto produce 11.03 g of slightly colored viscous liquid

출처 및 근거

ORD 기록
ord-6861fade62294d52a3952de686120f5a
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07625499B2

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