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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387284Generated: October 30, 2026

Hydrochloric Acid → 7-(1-Methylethyl)-1,4-dioxa-8-thiaspiro[4.5]decane

https://huagongshe.com/reaction/387284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorosuccinimideHCID 31398—
Reactant8-Thiabicyclo(3.2.1)octan-3-oneHCID 275054—
ReactantHCID 178418365HCID 178418365—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product7-(1-Methylethyl)-1,4-dioxa-8-thiaspiro[4.5]decaneHCID 5933273265.3%

Reaction Steps

N-Chlorosuccinimide (14.0 g, 104.9 mmol) was added in three portions with stirring over 15 min to a cooled (0° C.) solution of 8-thiabicyclo[3.2.1]octan-3-one (16.0 g, 99.9 mmol) in dry benzene (400 mL) under nitrogen. The mixture was stirred for a further 2.5 h and was then filtered. The filtrate was added dropwise with stirring under nitrogen to a cooled (0° C.) solution of isopropylmagnesium bromide (from isopropyl bromide (28.3 g, 229.7 mmol), magnesium (5.7 g, 234.7 mmol) and CuI (1.52 g, 7.9 mmol)) in dry ether (300 mL). The mixture was stirred for a further 15 h and cold (0° C.), dilute hydrochloric acid was added cautiously. The organic layer was separated and washed successively with water, saturated aqueous sodium bicarbonate, and finally with water again. The dried (Na2SO4) ether-benzene solution was evaporated, giving 13.2 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-fa49084830e04c329e9fd6df9519d1bf
Source noteuspto-grants-2013_02