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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863193Generated: October 25, 2026

Hydrochloric Acid → (R)-6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

https://huagongshe.com/reaction/863193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphateHCID 1061—
ReactantTriacetinHCID 5541—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylateHCID 13058283—
Solventtert-ButanolHCID 6386—
Product(R)-6-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 5135864741.4%

Reaction Steps

3 g (0.0136 mol) of methyl 6-methoxy-1,2,3,4-tetrahydro-2-naphthoate are dissolved in 100 ml of tert-butanol, and 300 ml of phosphate buffer at pH 7 are added to the solution prepared in this way. The pH of the solution, which rises to 7.3-7.5, is lowered to 7.1 by the addition of 1N HCl. 1.5 g of Sigma PPL enzyme (known as porcine pancreatic lipase type II, crude, Sigma L-3126--50 U/mg using triacetin) are added to the mixture. The pH tends to drop as the reaction progresses, but is kept constant by the addition of a 0.25N solution of NaOH, the pH being controlled by an automatic titration apparatus. After 4-5 hours, when about 22 ml of 0.25N NaOH have been consumed, sodium bicarbonate is added to the solution until the pH is 8 in order to stop the reaction by inactivation of the enzyme. Extraction is carried out with ethyl ether and the two phases are separated. The organic phase contains the unreacted ester principally of (S) configuration, which can be recovered as indicated in Example 2 below. The aqueous phase is acidified with concentrated sulfuric acid and the precipitate formed is filtered off to give 1.16 g of the title acid, which is crystallized from ethyl acetate. M.p. 130°-131° C.; [α]D20 =+57.8° (c=1.4%, CHCl3); ee 93.7% (HPLC performed under conditions (a)). This product is purer than that described in EP-A-436435, preparation (O) (i).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719308
Source datasetuspto-grants-1998_02
ORD IDord-5c335ec9e1e64ec0999ed4ec547b1943
Source noteuspto-grants-1998_02