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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353250Generated: October 27, 2026

tert-Butanol → (R)-4-Hydroxy-4-hydroxymethyl-6-chloro-8-difluoromethoxychromane

https://huagongshe.com/reaction/353250

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantSodium SulfiteHCID 24437—
Reactant1,4-Bis(dihydroquinidine)phthalazineHCID 11217202—
Reactant4-Methylene-6-chloro-8-difluoromethoxychromaneHCID 22708343—
SolventWaterHCID 962—
Product(R)-4-Hydroxy-4-hydroxymethyl-6-chloro-8-difluoromethoxychromaneHCID 6942877988%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of tert-butanol (46 mL) and water (46 mL) was added AD-mix-β (18.6 g). The mixture was cooled to 0° C. 4-Methylene-6-chloro-8-difluoromethoxychromane (3.2 g 12.97 mmol, see step (vi) above) in tert-butanol (11 mL) and water (11 mL) was added. The mixture was stirred at 0° C. for 24 h. Sodium sulfite (19.0 g, 150.74 mmol) was added, and the mixture was allowed to warm to room temperature and stirred for 1 h. The layers were separated and the aqueous phase was extracted with EtOAc (2×). The combined ethyl acetate phases were dried (Na2SO4) and evaporated. The crude product was chromatographed on silica gel, eluting with methylene chloride:ethyl acetate (4:6), to afford 3.2 g (88%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750243B1
Source datasetuspto-grants-2004_06
ORD IDord-d7c10adf2d43404c9a0b684a9241d702
Source noteuspto-grants-2004_06