Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3086Generated: October 28, 2026

Sodium Hydroxide → Trans-2,3,5,6,7,8-hexahydro-8-hydroxy-7-(N-propylamino)naphtho[2,3-b]thiophene

https://huagongshe.com/reaction/3086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTrans-2,3,5,6,7,8-hexahydro-8-hydroxy-7-propionylaminonaphtho[2,3-b]thiopheneHCID 70200501—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTrans-2,3,5,6,7,8-hexahydro-8-hydroxy-7-(N-propylamino)naphtho[2,3-b]thiopheneHCID 7020146097%

Reaction Steps

In a 500 ml three-necked flask fitted with a magnetic stirrer and a nitrogen inlet, 2.3 g (61 mmol) of AILiH4 are suspended in 75 ml of dry tetrahydrofuran. 6.2 g (24.5 mmol) of the product obtained in Step 2 dissolved in 97 ml of dry tetrahydrofuran are slowly added at room temperature. After 18 hours' stirring at room temperature, the reaction is stopped by the addition of 1.6 ml of water, 1.3 ml of 20 % NaOH in water and finally 5.8 ml of water in succession. The reaction mixture is stirred for 0.5 hour at room temperature and then filtered. The precipitate is washed copiously with tetrahydrofuran and the flitrate is concentrated in vacuo to yield 1.37 g of the expected product in the form of a meringue, Yield: 97 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733908
Source datasetuspto-grants-1998_03
ORD IDord-04b5894104d743daa3447f348afad5c1
Source noteuspto-grants-1998_03