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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331129Generated: October 27, 2026

Sodium Bicarbonate → (R)-5-(5-bromo-2-fluorophenyl)-6,6-difluoro-5,7,7-trimethyl-1,4-oxazepan-3-one

https://huagongshe.com/reaction/331129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTrimethylaluminumHCID 16682925—
Reactant(R)-ethyl 2-(4-amino-4-(5-bromo-2-fluorophenyl)-3,3-difluoro-2-methylpentan-2-yloxy)acetateHCID 58562965—
SolventTolueneHCID 1140—
Product(R)-5-(5-bromo-2-fluorophenyl)-6,6-difluoro-5,7,7-trimethyl-1,4-oxazepan-3-oneHCID 5856296897.8%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a solution of (R)-ethyl 2-(4-amino-4-(5-bromo-2-fluorophenyl)-3,3-difluoro-2-methylpentan-2-yloxy)acetate (intermediate B5.1) (6.85 g, 16.6 mmol) in toluene (205 ml) at 23° C. was added dropwise trimethylaluminum (2 M in toluene, 10.8 ml, 21.6 mmol) and the light yellow solution was stirred at 23° C. for 2 h. Poured into a saturated solution of sodium hydrogencarbonate, extracted with ethyl acetate, washed organic layer with brine, dried over sodium sulphate, filtered off and evaporated totally. Dried at high vacuum to give the (R)-5-(5-bromo-2-fluorophenyl)-6,6-difluoro-5,7,7-trimethyl-1,4-oxazepan-3-one (5.95 g, 16.2 mmol, 97.8% yield) as a light yellow solid, which was used without further purification. MS: m/z=366.2 [(M+H)+] and 368.1 [(M+2+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877744B2
Source datasetuspto-grants-2014_11
ORD IDord-6020c911733c4de2b055a63fcba9f394
Source noteuspto-grants-2014_11