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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497024Generated: November 1, 2026

Methanol → 2-Propanesulfinamide, 2-methyl-N-[(1S)-1,2,3,4-tetrahydro-5-(2,2,2-trifluoroethoxy)-1-naphthalenyl]-, [S(R)]-

https://huagongshe.com/reaction/1497024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium tri-s-butylborohydrideHCID 3611392—
ReactantHCID 89852658HCID 89852658—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2-Propanesulfinamide, 2-methyl-N-[(1S)-1,2,3,4-tetrahydro-5-(2,2,2-trifluoroethoxy)-1-naphthalenyl]-, [S(R)]-HCID 8985333043.2%

Reaction Steps

To a suspension of L-Selectride (3.90 mL, 3.90 mmol) in THF (1 mL) was added Intermediate 13A (0.45 g, 1.3 mmol) in THF (1 mL) at −50° C. The reaction mixture was warmed up to rt until the reduction was complete. To the reaction mixture was added MeOH (2 mL) and brine (2 mL). The resulting reaction mixture was stirred for 5 minutes, filtered, and the filtrate was concentrated in vacuo. The crude product was dissolved in a small amount of DCM and loaded on a 4 g silica gel cartridge eluting from 0 to 100% EtOAc in hexanes over 15 minutes to give Intermediate 13B (196 mg, 0.561 mmol, 43.1% yield). LCMS=2.09 min [M+1]=350 (Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199946B2
Source datasetuspto-grants-2015_12
ORD IDord-c76a0d2ebb1149f6a4eba20ff78349e1
Source noteuspto-grants-2015_12