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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324490Generated: October 29, 2026

Sodium borohydride → (+/-)-2,7-Dichloro-4H-benzo[5,6]cyclohepta[1,2-d]thiazol-4-ol

https://huagongshe.com/reaction/324490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2,7-Dichloro-4H-benzo[5,6]cyclohepta[1,2-d]thiazol-4-oneHCID 22003621—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(+/-)-2,7-Dichloro-4H-benzo[5,6]cyclohepta[1,2-d]thiazol-4-olHCID 70113755—

Reaction Steps

Sodium borohydride (0.159 g) was added to a suspension of the product from step (vi) (1.27 g) in methanol (20 ml) and dichloromethane (5 ml) at room temperature. After 3 h the mixture was partitioned between 2N NaOH and dichloromethane. The organic phase was collected, dried, (MgSO4) and solvent evaporated to leave a colourless foam. Yield: 1.27 g Used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218376B1
Source datasetuspto-grants-2001_04
ORD IDord-3730e788ac444b46a21c70c556d18e6f
Source noteuspto-grants-2001_04