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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83705Generated: October 25, 2026

Ammonium Chloride → (7-Chloro-1,3-dioxaindan-5-yl)methanol

https://huagongshe.com/reaction/83705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Chloro-1,3-dioxaindane-5-carbaldehydeHCID 676492—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product(7-Chloro-1,3-dioxaindan-5-yl)methanolHCID 4962440—

Reaction Steps

To a solution of 7-chlorobenzo[d][1,3]dioxole-5-carbaldehyde (6.0 g, 33 mmol) in THF (50 mL) was added NaBH4 (2.5 g, 64 mmol)) in portion at 0° C. The mixture was stirred at this temperature for 30 min and then poured into aqueous NH4Cl solution. The organic layer was separated, and the aqueous phase was extracted with EtOAc (50 mL×3). The combined extracts were dried over Na2SO4 and evaporated under reduced pressure to afford (7-chlorobenzo[d][1,3]dioxol-5-yl)methanol, which was directly used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846753B2
Source datasetuspto-grants-2014_09
ORD IDord-4aec2178fdcc41df98af1e562d44797c
Source noteuspto-grants-2014_09