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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426767Generated: October 30, 2026

Sodium borohydride → HCID 20389846, compound

https://huagongshe.com/reaction/426767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20389839HCID 20389839—
SolventEthanolHCID 702—
ProductHCID 20389846HCID 20389846—

Reaction Steps

24.6 g (0.1 mole) of 5-methyl-benzo[f]thieno[2,3-b]thiepin-4(5H)-one [see British Patent No. 1,334,538 and U.S. Pat. No. 3,682,959) is suspended in 350 ml of abs. ethanol, and to the suspension is added at 8°, with stirring, 3.8 g (0.1 mole) of sodium borohydride. The mixture is then stirred for 15 hours at room temperature. The clear solution is concentrated in vacuo, and the oily residue is taken up in methylene chloride. The solution is washed twice with water, dried over sodium sulphate and concentrated by evaporation, and the residue is dried in vacuo. The 4,5-dihydro-5-methyl-benzo[f]thieno[2,3-b]thiepin-4-ol thus obtained is a white, slightly sticky, solid mass, and is further processed as crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171366
Source datasetuspto-grants-1979_10
ORD IDord-96428edfda56473d92eac03c845d5fa4
Source noteuspto-grants-1979_10