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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241072Generated: October 31, 2026

HCID 86647829, compound → HCID 86647828, compound

https://huagongshe.com/reaction/241072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86647829HCID 86647829—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86647828HCID 8664782883%

Reaction Steps

To a cooled (0° C.) solution of 4-chloro-5,6,7,8-tetrahydroquinazoline-7-carbaldehyde (0.10 g, 0.51 mmol) in THF (5 mL) was added a solution of MeMgBr (3.0 M in ethyl ether, 0.40 mL, 1.2 mmol). The resulting mixture was stirred at ambient temperature for 30 minutes and then partitioned between ethyl acetate and saturated sodium bicarbonate. The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by silica gel chromatography provided 1-(4-chloro-5,6,7,8-tetrahydroquinazolin-7-yl)ethanol (0.09 g, 83% yield) as a waxy solid. MS (ES) for C10H13ClN2O: 213 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-65b80c6c8e814176b35be0519df91643
Source noteuspto-grants-2014_02