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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dichloromethane → 7-(Dimethoxythiophosphorylmethyl) naphthalene-1-carboxylic acid tert-butyl ester

HRID 496326
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HRID 496326 반응식
[P:1]([O-:6])([O:4][CH3:5])[S:2]C.[C:7]([O:11][C:12]([C:14]1[C:23]2[C:18](=[CH:19][CH:20]=[C:21]([CH2:24]Br)[CH:22]=2)[CH:17]=[CH:16][CH:15]=1)=[O:13])([CH3:10])([CH3:9])[CH3:8].[OH-].[Na+].Cl[CH2:29]Cl>[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.O>[C:7]([O:11][C:12]([C:14]1[C:23]2[C:18](=[CH:19][CH:20]=[C:21]([CH2:24][P:1]([O:6][CH3:29])([O:4][CH3:5])=[S:2])[CH:22]=2)[CH:17]=[CH:16][CH:15]=1)=[O:13])([CH3:10])([CH3:9])[CH3:8]
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참가 물질

7

반응물 4

HCID 6344DichloromethaneHCID 14798Sodium HydroxideHCID 121243517-Bromomethylnaphthalene-1-carboxylic acid tert-butyl esterHCID 86596782Dimethyl thiophosphite

생성물 1

HCID 697362767-(Dimethoxythiophosphorylmethyl) naphthalene-1-carboxylic acid tert-butyl ester

시약·촉매·용매 2

HCID 66133
Benzyl triethylammonium chloride
촉매
HCID 962Water용매

실험 절차

A solution of dimethyl thiophosphite (3.84 g, 30.5 mmol), crude 7-bromomethylnaphthalene-1-carboxylic acid tert-butyl ester (11.2 g, 34.9 mmol) and triethylbenzylammonium chloride (0.72 g, 3.17 mmol) in dichloromethane (100 mL) was cooled on an ice bath and a solution of sodium hydroxide (12.7 g, 0.317 mol) in water (12.7 mL) was added slowly with vigorous stirring. The ice bath was then removed and the mixture stirred overnight. The next morning, it was washed with water, dried (magnesium sulfate), and the solvent removed under reduced pressure to give crude 7-(dimethoxythiophosphorylmethyl) naphthalene-1-carboxylic acid tert-butyl ester (See FIG. 1) (10.38 g) as orange oil.

후처리

  1. customThe ice bath was then removed
  2. washThe next morning, it was washed with water
  3. dry with materialdried (magnesium sulfate)
  4. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-a1335bbf37fd4126b76753cf24cfda59
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943267B1

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