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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183710Generated: October 26, 2026

Water → 1,1-Dimethylethyl 3,4-dihydro-5-(hydroxymethyl)-2(1H)-isoquinolinecarboxylate

https://huagongshe.com/reaction/2183710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantTert-butyl 5-formyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylateHCID 22335239—
SolventMeOH tetrahydrofuranHCID 21899815—
Product1,1-Dimethylethyl 3,4-dihydro-5-(hydroxymethyl)-2(1H)-isoquinolinecarboxylateHCID 6956121668.8%

Reaction Steps

To solution of 5-formyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 20a (0.44 g, 1.71 mmol) in 40 mL of methanol:tetrahydrofuran (1:1) at room temperature was added sodium borohydride (0.072 g, 1.88 mmol), and the mixture was stirred to room temperature for 3 h. Water (30 mL) was added followed by ammonium chloride saturated solution (20 mL) and the product was extracted with dichloromethane. The combined organics were dried over magnesium sulfate, the solvent was evaporated and the residue was purified by flash chromatography eluting with 30% ethyl acetate in hexanes, to yield 0.31 g of 5-hydroxymethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 21a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900220B2
Source datasetuspto-grants-2005_05
ORD IDord-ec7013c37b2e49daa4d7055202097742
Source noteuspto-grants-2005_05