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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229450Generated: November 1, 2026

Hydrochloric Acid → HCID 18467612, compound

https://huagongshe.com/reaction/2229450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-tert-butylmethanesulfonamideHCID 4130162—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18467612HCID 18467612—

Reaction Conditions

Temperature5 °C

Reaction Steps

A 2.0 M solution of lithium diisopropylamide in heptane/tetrahydrofuran/ethylbenzene (400 ml) was cooled to −45 to −50° C. under nitrogen atmosphere. A solution (100 ml) of N-t-butylmethanesulfonamide (55.0 g) in tetrahydrofuran was added dropwise thereto for 20 minutes. After raising the temperature to 5° C. taking 1 hour, the solution was cooled again to −65° C. To the resulting solution was added dropwise a solution of n-butyl aldehyde (28.8 g) in tetrahydrofuran (100 ml) for 30 minutes. The solution was stirred for 18 hours while raising the temperature gradually to room temperature. The resulting reaction solution was poured into an excess amount of dilute hydrochloric acid under cooling with ice to make it acidic and extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulfate, and concentrated under reduced pressure to obtain a solid crude product. Hexane (300 ml) was added thereto with stirring. Crystals thus obtained were collected by filtration, washed with hexane, and dried under reduced pressure to obtain N-t-butyl-2-hydroxy-1-pentane-sulfonamide (46.2 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420409B1
Source datasetuspto-grants-2002_07
ORD IDord-66559e9487294bc283d153f62b96ef70
Source noteuspto-grants-2002_07