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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763903Generated: November 1, 2026

Triethylamine → HCID 12761811, compound

https://huagongshe.com/reaction/1763903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Aminomethyl-4-t-butyl-6-iodophenolHCID 119286—
ReactantHCID 86585469HCID 86585469—
SolventWaterHCID 962—
ProductHCID 12761811HCID 12761811—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 2-aminomethyl-4-(1,1-dimethylethyl)-6-iodophenol (12 g., 0.04 mole) in tetrahydrofuranwater (10:3; v:v; 130 ml.) is added 1,1-dimethylethyl-2,4,5-trichlorophenyl carbonate (13 g., 0.044 mole) and triethylamine (4.44 g., 0.044 mole). The resulting pale yellow solution is stirred and heated at 60°-65° C. for 24 hours, cooled to 20° C. and diluted with water (700 ml.). The solid which precipitates is collected, air-dried, triturated with petroleum ether and dried to give 1,1-dimethylethyl N-[2-hydroxy-3-iodo-5-(1,1-dimethylethyl)phenylmethyl]carbamate as a colorless solid (14.3 g., 88%), m.p. 196°-197° with dec. Recrystallization from ethyl acetate affords an analytical sample of 1,1-dimethylethyl N-[2-hydroxy-3-iodo-5-(1,1-dimethylethyl)phenylmethyl]carbamate as colorless crystals, m.p. 199°-200° with dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113877
Source datasetuspto-grants-1978_09
ORD IDord-ad7b2431712a48b0b285fc47c309778d
Source noteuspto-grants-1978_09