Production Method 1

98-03-3

636-72-6

155669-26-4

874-83-9

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Potassium carbonate ,  (OC-6-42)-[1,1′-(1,4-Butanediyl)bis[1,1-diphenylphosphine-κP]]dichloro(2-pyridin… Solvents: Isopropanol ;  3 h, 82 °C

Reference

Transfer Hydrogenation and Hydrogenation of Commercial-Grade Aldehydes to Primary Alcohols Catalyzed by 2-(Aminomethyl)pyridine and Pincer Benzo[h]quinoline Ruthenium Complexes

Baldino, Salvatore; et al, ChemCatChem, 2016, 8(13), 2279-2288

Thiophen-2-ylmethanol Raw materials

• Thiophene-2-carbaldehyde

Thiophen-2-ylmethanol Preparation Products

• (1E,4E)-1,5-Di(2-thienyl)-1,4-pentadien-3-one (155669-26-4)
• 4-(2-Thienyl)but-3-en-2-one (874-83-9)
• Thiophen-2-ylmethanol (636-72-6)

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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Heteroaromatic compounds Heteroaromatic compounds
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Heteroaromatic compounds

• 30689-48-6(Naphtho[2,1-b]thiophene-2-methanol)
• 63826-59-5((5-methylthiophen-2-yl)methanol)
• 6007-86-9(thiophene-2,5-diyldimethanol)
• 13679-76-0(2-Thiophenemethanol, formate)
• 1487-28-1(Thiophene, 2-(methoxymethyl)-)
• 827017-58-3(Thiophene, methoxymethyl-)
• 13679-77-1(2-Thiophenemethanol, acetate)
• 17890-56-1(2-(Hydroxymethyl)benzobthiophene)
• 88045-59-4(2-Thiophenemethanol, sodium salt)
• 74395-18-9((4-Methylthiophen-2-yl)methanol)