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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67056Generated: October 27, 2026

Benzyl Alcohol → Benzyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride

https://huagongshe.com/reaction/67056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
Reactant1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acidHCID 95489—
SolventDiethyl EtherHCID 3283—
ProductBenzyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochlorideHCID 20273210—

Reaction Conditions

Temperature90 °C

Reaction Steps

Benzyl alcohol, 750 ml, was treated with 150 g of commercial polyphosphoric acid and warmed and stirred at 90° C. to obtain a homogeneous mixture. Solid 1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid (S-form) 165.2 g was added. The mixture was stirred 4 hours at 95°-105° C. and then allowed to stand at room temperature for 18 hours. A solution of 18.5 g gaseous hydrochloric acid in 2.5 l of anhydrous ether was added, and the product separated slowly on cooling overnight. Filtration gave the crude benzyl 1,2,3,4-tetrahydro-3-isoquinoline carboxylate hydrochloride. This was purified by recrystallization from ethanol twice to give material with mp 190.5°-191° C.; [α]D 23=-83.3° (1% 1:1 methanol/1 N hydrochloric acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344949
Source datasetuspto-grants-1982_08
ORD IDord-d41cb35c3c15423083594c06b142ee98
Source noteuspto-grants-1982_08