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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492985Generated: October 25, 2026

1-(Chloromethoxy)-2-methoxyethane → 3,5-Bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzonitrile

https://huagongshe.com/reaction/1492985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantBenzonitrile, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-HCID 137274—
ReactantN,N-DiisopropylmethylamineHCID 547370—
SolventDichloromethaneHCID 6344—
Product3,5-Bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzonitrileHCID 1004164397%

Reaction Steps

2-Methoxyethoxymethyl chloride (4.1 g, 0.032 mole) is added dropwise to a 0° C. mixture of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzonitrile (Louis A. Cohen, Journal of Organic Chemistry 22, 1333, 1957) (5.0 g, 0.022 mole) and diisopropylaminomethane (4.2 g, 0.032 mole) in methylene chloride (50 ml). The mixture is allowed to warm to room temperature and stir 18 hours. The solution is diluted with methylene chloride (25 ml) and washed with water (25 ml), cold 2M HCl (20 ml), saturated aqueous NaCl, and dried over MgSO4. Filtered and concentrated in vacuo to obtain 6.7 g (6.9 g theor., 97%) of 3,5-bis(1,1-dimethylethyl)-4-[(2-methoxyethoxy)methoxy]benzonitrile as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05376670
Source datasetuspto-grants-1994_12
ORD IDord-72dea649b3064f1ab34284d1e0480de1
Source noteuspto-grants-1994_12