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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652435Generated: October 30, 2026

Sodium borohydride → HCID 13808652, compound

https://huagongshe.com/reaction/652435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13808651HCID 13808651—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13808652HCID 1380865284.4%

Reaction Steps

To a solution of 4-(3-chloropropyl)-7-methoxy-3,4-dihydro-2H-1,5-benzoxathiepin-3-one (0.8 g) in tetrahydrofuran (2 ml) and methanol (10 ml) is added sodium borohydride (0.1 g) under ice-cooling. The reaction mixture is stirred for another one hour and evaporated in vacuo. The residue is mixed with ethyl acetate and water. The orgonic layer is separated, washed with water, dried over anhydrous sodium sulfate and evaporated to dryness in vacuo. The residue is submited to column chromatography on silica gel eluting with ethyl acetate-hexane (1:1) to give 4-(3-chloropropyl)-7-methoxy-3,4-dihydro-2H-1,5-benzoxathiepin-3-ol (0.68 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04672064
Source datasetuspto-grants-1987_06
ORD IDord-94988ebe73bc42a186ce17d5154ca02f
Source noteuspto-grants-1987_06