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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330268Generated: October 25, 2026

1-Chloro-3,4-dihydronaphthalene-2-carboxaldehyde → (1-Chloro-3,4-dihydronaphthalen-2-yl)methanol

https://huagongshe.com/reaction/330268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3,4-dihydronaphthalene-2-carboxaldehydeHCID 76752—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(1-Chloro-3,4-dihydronaphthalen-2-yl)methanolHCID 14819335102.2%

Reaction Steps

To a mixture of sodium borohydride (2.83 g, 0.075 mol) in methanol (150 mL) at 0° C., was added dropwise a solution of 1-chloro-2-formyl-3,4-dihydronaphthalene (9.59 g, 0.05 mol) in dry THF (150 mL). The reaction was stirred at room temperature for 1 hour, carbon dioxide was cautiously bubbled through the reaction mixture for 15 minutes, and the resulting mixture was concentrated under reduced pressure. The residue was diluted with water (150 mL), extracted with ether (3×150 mL), dried (MgSO4) and concentrated to give 9.95 g (102%) of product as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895860
Source datasetuspto-grants-1990_01
ORD IDord-a203c78374d04dca998de492e3dae3ff
Source noteuspto-grants-1990_01