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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120095Generated: November 1, 2026

Sodium borohydride → HCID 12096237, compound

https://huagongshe.com/reaction/2120095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12046097HCID 12046097—
SolventFormic AcidHCID 284—
ProductHCID 12096237HCID 1209623760%

Reaction Steps

7-bromo-2-(1,1-dimethylethyl)-2,3-dihydro-1,2-benzisothiazol-3-ol 1,1-dioxide (1.4 g, 4.4 mmol) was treated with formic acid (10 mL). The reaction was stirred at ambient temperature over 18 h, concentrated in vacuo and dissolved in methanol (10 mL). The mixture was cooled to 0° C. and treated with sodium borohydride (0.17 g, 4.4 mmol) in small portions over 20 min. The cooling bath was removed and the resulting reaction mixture stirred at ambient temperature over 18 h. The work-up consisted of slowly quenching the reaction mixture with ice, dilution with water and extraction with ethyl acetate. Drying over sodium sulfate and concentrating under reduced pressure provided the crude product that was purified by a plug of silica gel (ethyl acetate/hexane, 1:4) to afford the desired 7-bromo-2,3-dihydro-1,2-benzisothiazole 1,1-dioxide (0.6 g, 60% over 2 steps). 1H NMR (CD3OD): δ 4.40 (s, 2H), 7.53 (m, 2H), 7.70 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689770B2
Source datasetuspto-grants-2004_02
ORD IDord-f56605e438564dce8c22865dbdf3b224
Source noteuspto-grants-2004_02