Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016755Generated: October 31, 2026

2-Bromoethanol → 94283-73-5

https://huagongshe.com/reaction/1016755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
Reactant3-(2-Hydroxyethoxy)-4-(1-methylethoxy)benzaldehydeHCID 22039918—
Product94283-73-5HCID 1545352175%

Reaction Steps

from 3-hydroxy-4-isopropoxybenzaldehyde (prepared in 75% yield by monoalkylation of 3,4-dihydroxybenzaldehyde with isopropyl bromide and K2CO3 in DMF) and 2-bromoethanol there was obtained 3-(2-hydroxy-ethoxy)-4-isopropoxy-benzaldehyde, which was subsequently converted by reaction with 4-aminobenzonitrile and toluene-4-sulphonyl methylisocyanide into methyl (RS)-(4-cyano-phenylamino)-[3-(2-hydroxy-ethoxy)-4-isopropoxy-phenyl]-acetate and then into methyl (RS)-(4-carbamimidoyl-phenylamino)-[3-(2-hydroxy-ethoxy)-4-isopropoxy-phenyl]-acetate hydrochloride (1:1);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476264B2
Source datasetuspto-grants-2002_11
ORD IDord-4d7d6d7e249a40f68fcc08ef6ccfcdef
Source noteuspto-grants-2002_11