Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013156Generated: October 25, 2026

Sodium borohydride → Benzenemethanol,2-benzo[b]thien-5-yl-

https://huagongshe.com/reaction/1013156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantBenzaldehyde,2-benzo[b]thien-5-yl-HCID 60139760—
SolventMethanolHCID 887—
ProductBenzenemethanol,2-benzo[b]thien-5-yl-HCID 6013974393.7%

Reaction Steps

To a suspension of 2-Benzo[b]thiophene-5-yl-benzaldehyde (compound PRE14) (3.31 g, 13.9 mmole) in methanol (30 mL) was added at 0-5° C. portionwise NaBH4 (0.528 g, 13.9 mmole). At the end of the addition, the cooling bath was removed and the reaction mixture was stirred at room temperature for 2 h. After concentration, the residue was diluted with water and diethyl ether, the organic layer dried over Na2SO4 and concentrated to give 3.13 g of compound O7 as an orange brown oil (Yield=94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981907B2
Source datasetuspto-grants-2011_07
ORD IDord-e122286ac6eb4b5e8633c656314d250f
Source noteuspto-grants-2011_07