反応 #4156944
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e11d3bd28fa5488bb6e4a4bb9b0a8a5b表示可能な構造データがありません
CSC1=CC=C(C=C1)C=O製品情報
4-methylsulfanylbenzaldehyde (CAS 3446-89-7) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 76985
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e11d3bd28fa5488bb6e4a4bb9b0a8a5b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-4c7b02c9bc924ea29aa1f26fb8360e5d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c18973ca12aa48ef9caaebeb25e63275反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-599ad40d588b4adf9d5799dbc62df121反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-58ecc0ba482c46e993fd19190e28dde2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e1c040c0d38443ae993f3df1f6d4865c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-52474126398f41af832fbeb85705a02c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-675e3fd9074d4b26b4e1647d7875c56f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a manner analogous to Preparation 1, tosylmethylisocyanide (0.23 g, 1.20 mmol), 4-(methylthio)benzaldehyde (0.19 g, 1.26 mmol), and NaCN (5.9 mg, 0.12 mmol) gave the desired compound as a tan solid. MS(ES+) m/z 348.4 (M+H+).
ソース ID: ord-d6d778ebffa549d5bc8269845550ea25反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a solution of triethyl 2-phosphonopropionate (47 g, 0.19 mol) in THF (200 mL) was added solid magnesium bromide etherate (59 g, 0.23 mol) under nitrogen. Triethylamine (26.5 mL, 0.19 mol) was added after 5 min. The mixture was stirred for 10 min and 4-(methylthio)benzaldehyde (27.1 mL, 0.19 mol) was added. After 15 h at room temperature the mixture was diluted with water (400 mL) and hexane (400 mL). The two layers were separated. The organic layer was washed with water (400 mL), dried over 4 Å molecular sieves, filtered, and concentrated to give 42.5 g (95%) of ester 6a as a light yellow oil: IR (neat) 2980, 1705, and 1240 cm-1 ; 1H NMR (CDCl3, 300 MHz) δ 7.63 (1 H), 7.33 (2 H), 7.25 (2 H), 4.26 (2 H), 2.50 (3 H), 2.12 (3 H), and 1.34 (3 H); 13C NMR (CDCl3, 75.5 MHz) δ 168.71, 139.37, 138.08, 132.55, 130.19, 127.98, 125.89, 60.87, 15.38, 14.37 and 14.17. The two layers were separated The organic layer was washed with water (400 mL) dried over 4 Å molecular sieves filtered concentrated
ソース ID: ord-11c045263ed64978a107e051f15eea11反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 7.6 g of 4-methylmercaptobenzaldehyde, 16 g of γ-methoxyacetoacetic acid ethyl ester and 6 ml of aqueous concentrated ammonia in 30 ml of ethanol are heated to the boil for 6-8 hours, and 2,6-dimethoxymethyl-4-(4'-methylmercaptophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester is obtained in the form of beige crystals of melting point 136°-138° C.
ソース ID: ord-73b84b635c304d208b0b8b973465f8bb反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e11d3bd28fa5488bb6e4a4bb9b0a8a5bPubChem References
化合物の公開データベース記録に掲載された情報源です。
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