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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742419Generated: November 1, 2026

Sodium borohydride → HCID 53845926, compound

https://huagongshe.com/reaction/1742419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22755584HCID 22755584—
SolventMethanolHCID 887—
ProductHCID 53845926HCID 5384592684.3%

Reaction Steps

To a solution of acetic acid 1-oxo-indan-5-yl ester (2700 mg, 14.2 mmol) in MeOH (20 mL) at 0° C. was added sodium borohydride (760 mg, 20 mmol). The reaction mixture was stirred for 2 hours, quenched with saturated aqueous NH4Cl (20 mL) and diluted with ethyl acetate (500 mL). The organic solution was washed with saturated aqueous NaHCO3 (50 mL) and saturated aqueous NaCl (50 mL), dried (Na2SO4) and concentrated in vacuo to give 2.3 grams of the desired product. 1H NMR (250 MHz, CDCl3): d 7.35 (d, 2 H), 6.90 (m, 2 H), 5.2 (t, 1 H), 3.0 (m, 1 H), 2.8 (m, 1 H), 2.5 (m, 1 H), 2.3 (s, 3 H), 1.95 (1 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338740
Source datasetuspto-grants-1994_08
ORD IDord-a782773c85e04e8bb3bce2113b80cf34
Source noteuspto-grants-1994_08