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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 1,4-Bis(dihydroquinidine)phthalazine | HCID 11217202 | — |
| Reactant | 4-Methylene-6-chloro-8-difluoromethoxychromane | HCID 22708343 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-4-Hydroxy-4-hydroxymethyl-6-chloro-8-difluoromethoxychromane | HCID 69428779 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750243B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-d7c10adf2d43404c9a0b684a9241d702 |
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| Source note | uspto-grants-2004_06 |
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